Responsible for driving to ensure product development is completed on schedule, within budget and with prestigious quality ensuring development is completed on schedule and budget.\u003C/p>\u003Cp>\u003C/p>\u003Cp>\u003Cb>Essential Functions\u003C/b>\u003Cbr />• Supervision and Coordination of Offshore Development Resources (60%)\u003Cbr />• Review requirements and provide feedback to Project Managers and coordinate understanding to the vendors\u003Cbr />• Provide code reviews to contribute to continuous improvement\u003Cbr />• Escalate time, cost or quality implications to project manager and development manager\u003Cbr />• Lead technical knowledge transfer where necessary\u003Cbr />• Analyze existing solutions to provide recommendations on improvements\u003Cbr />• Collaborate with team members to develop and maintain suitable coding standards\u003Cbr />• Attend personal training for at least one week per half year to improve skills\u003Cbr />• Contribute to project effort estimations\u003C/p>\u003Cp>\u003C/p>\u003Cp>\u003Cb>Our ideal Candidate Will Have\u003C/b>\u003C/p>\u003Cp>- 5+ years of experience in software development (any stack)\u003C/p>\u003Cp>- Excellent coding and software development skills in Python\u003C/p>\u003Cp>- Knowledge of JavaScript/TypeScript and familiarity with a UI framework (preferably React)\u003C/p>\u003Cp>- Familiarity with designing and using RESTful APIs\u003C/p>\u003Cp>- Good understanding of databases and best practices around data management\u003C/p>\u003Cp>- Experience writing unit and integration tests\u003C/p>\u003Cp>- Previous experience working within an agile environment\u003C/p>\u003Cp>\u003C/p>\u003Cp>We know that meaningful results require not only the right approach but also \u003Cb>the right people\u003C/b>. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and\u003C/p>\u003Cp>\u003Cb>Whatever your career goals, we are here to ensure you get there!\u003C/b>\u003C/p>\u003Cp>\u003Cb>We invite you to join IQVIA™.\u003C/b>\u003C/p>\u003Cp>\u003C/p>\u003Cp>At IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 70,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way. Learn more at \u003Ca href=\"http://jobs.iqvia.com\" target=\"_blank\">jobs.iqvia.com\u003C/a>.\u003C/p>","https://iqvia.wd1.myworkdayjobs.com/iqvia/job/London-United-Kingdom/Full-Stack-Developer_R1220214",{"id":67,"name":68,"urlSafeSlug":68,"logo":69},[99],{"city":100,"region":101,"country":102},"London","England","United Kingdom","2021-07-22T00:00:00Z",28,"Candidates should possess 5+ years of experience in software development across various stacks, along with excellent coding and software development skills in Python. Familiarity with JavaScript/TypeScript and UI frameworks, particularly React, is required, as is experience designing and utilizing RESTful APIs. A strong understanding of databases and data management best practices is also necessary, alongside previous experience working within an agile environment and a proven ability to write unit and integration tests.","The Full Stack Developer will supervise and coordinate offshore development resources, review requirements and provide feedback to project managers, conduct code reviews to contribute to continuous improvement, escalate time, cost, or quality implications to project managers and development managers, lead technical knowledge transfer where necessary, analyze existing solutions to provide recommendations on improvements, and collaborate with team members to develop and maintain suitable coding standards. They will also attend personal training to improve skills and contribute to project effort estimations.",1,{"employment":109,"compensation":114,"experience":118,"visaSponsorship":124,"location":125,"skills":126,"industries":136},{"type":110},{"id":111,"name":112,"description":113},"7b45c8cf-5aad-4473-9b42-e655134195c8","Full Time","Commit to a standard 40-hour workweek, usually with full benefits.",{"minAnnualSalary":115,"maxAnnualSalary":116,"currency":117,"details":18},60000,100000,"GBP",{"experienceLevels":119},[120],{"id":121,"name":122,"description":123},"6d29fb0e-c389-4488-940b-7ca93a9f10bb","Junior (1 to 2 years)","Gain initial job experience and develop your skills.",{"type":48},{"type":48},[127,128,129,130,131,132,133,134,135],"Python","JavaScript","TypeScript","React","RESTful APIs","Databases","Unit Testing","Integration Testing","Agile",[137,138],{"id":66,"name":65},{"id":139,"name":140},"00000000-0000-0000-0000-000000000000","Pharmaceuticals",{"id":142,"title":143,"alternativeTitles":144,"slug":160,"jobPostId":142,"description":161,"applyUrl":162,"company":68,"companyOption":163,"locations":164,"listingDate":169,"listingSite":104,"isRemote":55,"requirements":170,"responsibilities":171,"status":107,"expiryDate":18,"summary":172},"c6d95150-6e76-4d46-b5bd-babe940254ce","Project Manager - IM",[145,146,147,148,149,150,151,152,153,154,155,156,157,158,159],"Information Management Project Lead","IM Delivery Manager","Pharmaceutical IM Project Manager","Healthcare IM Consultant","Life Sciences Project Manager - IM","IM Solutions Delivery Manager","Client-Facing IM Project Manager","Technical Project Manager - IM","IM Service Delivery Lead","Pharma IM Implementation Manager","Healthcare Information Management Lead","Life Sciences IM Program Manager","IM Business Development Project Manager","Consulting Project Manager - IM","IM Technical Lead","project-manager-im-c6d95150-6e76-4d46-b5bd-babe940254ce","## Job Overview\nResponsible for the on-time completion of service delivery, managed services, or implementation oriented client projects. Manages a cross-functional team (onshore/ offshore) to achieve project delivery success. Identifies and elevates potential new business opportunities. Provides Technical Leadership to the project team.\n\n## Essential Functions\n- Participates/leads teams in the design, development and delivery of technology/service based projects or components of larger, complex projects.\n- Reviews and analyzes client requirements/problems.\n- Proposes and delivers cost effective solutions to meet these requirements.\n- Performs qualitative/quantitative analyses to assist in the identification of client issues and develop client specific solutions.\n- Designs, structures and delivers client reports and presentations.\n- Recommends improvements and alternative solutions.\n- Provides follow-up with internal and/or external client to ensure client satisfaction.\n- Proactively develops broader and deeper knowledge of technology/services solutions and trends for the pharmaceutical/healthcare/life sciences market.\n- Begins to develop practice specific subject matter expertise, either in technology & applications consulting or functional areas for the pharmaceutical/healthcare/life sciences industry.\n- Ability to manage work streams, assigning tasks and driving them to completion. May assist with business development activities.\n\n## Qualifications\n- Bachelor's Degree\n- 5–8 years of related experience in consulting or services delivery, ideally in pharmaceutical/healthcare/life sciences industry\n- Solid project management, client influencing and relationship building skills.\n- Strong technical architecture / design or development experience desired.\n- Works willingly and effectively with others in and across the organization to accomplish team goals.\n- Experienced with developing consultative relationships with senior level managers and executives at clients in the pharmaceutical/healthcare/life sciences industry.\n- Ability to manage multiple projects, juggle priorities and deliver on tight deadlines.\n- Knowledge of consulting methodologies, tools and techniques related to functional area.\n- Knowledge of key issues and current developments in the industry.\n- Excellent presentation, communication and client influencing skills.\n- Has established network and referral contacts.\n- Has necessary subject matter expertise to effectively manage projects within a given CoE.\n\n## About IQVIA\nAt IQVIA, we believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. The advanced analytics, technology solutions and contract research services we provide to the life sciences industry are made possible by our 70,000+ employees around the world who apply their insight, curiosity and intellectual courage every step of the way.","https://iqvia.wd1.myworkdayjobs.com/iqvia/job/Madrid-Spain/Project-Manager---IM_R1245629",{"id":67,"name":68,"urlSafeSlug":68,"logo":69},[165],{"city":166,"region":167,"country":168},"Madrid","Community of Madrid","Spain","2021-11-02T00:00:00Z","Candidates should possess a Bachelor's Degree and 5–8 years of related experience in consulting or services delivery, ideally within the pharmaceutical, healthcare, or life sciences industry. They should demonstrate solid project management skills, client influencing abilities, and strong technical architecture or development experience. Furthermore, candidates must have experience in developing consultative relationships with senior-level managers and executives at clients, and be knowledgeable about consulting methodologies, tools, and techniques related to functional areas, as well as key issues and current developments within the industry.","The Project Manager - IM will be responsible for the on-time completion of service delivery, managed services, or implementation-oriented client projects, managing a cross-functional team to achieve project delivery success. They will identify and elevate potential new business opportunities, provide technical leadership to the project team, participate in the design and delivery of technology/service-based projects, analyze client requirements and propose cost-effective solutions, deliver client reports and presentations, recommend improvements, and provide follow-up with clients to ensure satisfaction. Additionally, they will proactively develop knowledge of technology/services solutions and trends, assist with business development activities, manage work streams, and assign tasks to ensure project completion, while also beginning to develop practice-specific subject matter expertise.",{"employment":173,"compensation":175,"experience":176,"visaSponsorship":181,"location":182,"skills":183,"industries":198},{"type":174},{"id":111,"name":112,"description":18},{"minAnnualSalary":18,"maxAnnualSalary":18,"currency":18,"details":18},{"experienceLevels":177},[178],{"id":179,"name":180,"description":18},"9f0ed8d0-b24f-43cb-84c3-62a181e19994","Senior (5 to 8 years)",{"type":48},{"type":107},[184,185,186,187,188,189,190,191,192,193,194,195,196,197],"Project Management","Client Relationship Management","Technical Leadership","Service Delivery","Consulting","Pharmaceutical Industry","Healthcare Industry","Life Sciences Industry","Team Management","Client Influencing","Technical Architecture","Solution Design","Client Reporting","Presentation Skills",[199,201,202],{"id":139,"name":200},"Pharmaceutical",{"id":66,"name":65},{"id":139,"name":203},"Life Sciences",{"id":205,"title":206,"alternativeTitles":207,"slug":218,"jobPostId":205,"description":219,"applyUrl":220,"company":68,"companyOption":221,"locations":222,"listingDate":224,"listingSite":104,"isRemote":55,"requirements":225,"responsibilities":226,"status":107,"expiryDate":18,"summary":227},"58c223d6-65bd-4648-94be-f2e208994cde","Sales Rep Sevilla, Huelva, Cádiz y Córdoba",[208,209,210,211,212,213,214,215,216,217],"Life Sciences Sales Representative Sevilla","Medical Sales Specialist Huelva","Pharmaceutical Sales Executive Cádiz","Biotech Sales Professional Córdoba","Regional Sales Manager Life Sciences Andalusia","Territory Sales Executive Sevilla","Healthcare Sales Representative Huelva","Clinical Sales Specialist Cádiz","Life Science Account Manager Córdoba","Sales Executive Andalusia Region","sales-rep-sevilla-huelva-cadiz-y-cordoba-58c223d6-65bd-4648-94be-f2e208994cde","## About IQVIA\nIQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world. Learn more at jobs.iqvia.com\n\n## Employment Type\n* Full time","https://iqvia.wd1.myworkdayjobs.com/iqvia/job/Madrid-Spain/Sales-Rep-Sevilla--Huelva--Cdiz-y-Crdoba_R1281866",{"id":67,"name":68,"urlSafeSlug":68,"logo":69},[223],{"city":166,"region":167,"country":168},"2022-03-02T00:00:00Z","The ideal candidate should possess a strong sales acumen and experience within the life sciences industry, though specific educational requirements are not explicitly stated. Demonstrated ability to navigate and effectively cover the regions of Sevilla, Huelva, Cádiz, and Córdoba is essential.","As a Sales Representative at IQVIA, you will be responsible for identifying and pursuing new business opportunities within the designated geographic regions, building and maintaining strong relationships with key clients, and achieving sales targets. You will also contribute to the overall growth of IQVIA by proactively engaging with potential customers and presenting the company’s solutions effectively.",{"employment":228,"compensation":230,"experience":231,"visaSponsorship":236,"location":237,"skills":238,"industries":239},{"type":229},{"id":111,"name":112,"description":18},{"minAnnualSalary":18,"maxAnnualSalary":18,"currency":18,"details":18},{"experienceLevels":232},[233],{"id":234,"name":235,"description":18},"d9dd41a2-3551-412f-981e-de2bc1e7bb34","Mid-level (3 to 4 years)",{"type":48},{"type":107},[],[240,241,242],{"id":139,"name":203},{"id":66,"name":65},{"id":63,"name":62},{"id":244,"title":245,"alternativeTitles":246,"slug":257,"jobPostId":244,"description":258,"applyUrl":259,"company":68,"companyOption":260,"locations":261,"listingDate":263,"listingSite":104,"isRemote":55,"requirements":264,"responsibilities":265,"status":107,"expiryDate":18,"summary":266},"09f26b6f-cb1a-4907-864b-e34dda714397","Life & Science Recent Graduate - Italian Native Speaker",[247,248,249,250,251,252,253,254,255,256],"Medical Device Data Specialist - Italian Speaker","Pharmaceutical Data Analyst - Italian Native","Life Science Data Management Graduate - Italian","Product Data Steward - Italian Native Speaker","Medical Device Information Specialist - Italian","Global Product Data Coordinator - Italian","Life Science Data Entry Specialist - Italian","Pharmaceutical Reference Data Associate - Italian","Medical Device Data Operations Graduate - Italian","Life Science Product Information Analyst - Italian","life-science-recent-graduate-italian-native-speaker-09f26b6f-cb1a-4907-864b-e34dda714397","## About IQVIA\nIQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.\n\n## Role Overview\nWe are seeking L&S graduates to join our Medical Devices team. If you want to play a key role in a multicultural, dynamic and committed fun team this could be the role for you!\n\n## Key Responsibilities\n- Set up and Maintenance of Global Medical Devices Product data.\n- Perform data research to gather information on product attributes.\n- Identify when and how to correct inaccurate data, delete data, or add new entries to make the reference files more complete.\n- Receive input to the reference process from manufacturers.\n- Validate that the information gathered represents accurate new data and recommends changes, additions, or deletions in IQVIA’ existing reference data.\n- Identify required changes to the existing reference file.\n- Update IQVIA reference file(s) and databases.\n- Produce files and outputs for specified production and quality control processes, client support activities, etc.\n- Respond to queries on reference data (as required), referring difficult queries to team leader.\n\n## Required Knowledge, Skills and Abilities\n- Bachelor of Science and/or related experience.\n- Good PC literacy skills, including Word, and Excel.\n- Ability to carry out some analysis and information gathering to resolve problems on routine matters.\n- Developing knowledge of the company's products and pharmaceutical industry.\n\n## Employment Type\n- Full time\n\n## About IQVIA - Awards and Recognition\n- Recognized by Great Place to Work as the third best company to work for in Spain (March 2020).\n- FORTUNE Magazine's World's Most Admired Companies list for the third year in a row (January 2020).\n- Recognized by the 2016 Scrip Awards as the Best Full-service Provider Contract Research Organization (CRO).\n- Awarded the 2016 Eagle Award from the Society for Clinical Research Sites (SCRS) for the fourth consecutive year.\n- A site-nominated award recognizing contract research organizations (CRO) and biopharmaceutical sponsors dedicated to building positive relationships with research sites through leadership, professionalism and integrity.\n- IQVIA™ named in The International Association of Outsourcing Professionals (IAOP) 2017 Global Outsourcing 100® List which recognizes the world’s best service providers across a range of industries.\n\n## Our Commitment\nIQVIA™ is an equal opportunity employer. We make employment decisions based on qualifications and merit. We prohibit discrimination based on any unlawful consideration such as age, race, national origin, gender or other \"protected status.\"\n\nWe know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and whatever your career goals, we are here to ensure you get there!\n\nIQVIA is a leading global provider of advanced analytics, technology solutions and clinical research services to the life sciences industry. We believe in pushing the boundaries of human science and data science to make the biggest impact possible – to help our customers create a healthier world.","https://iqvia.wd1.myworkdayjobs.com/iqvia/job/Madrid-Spain/Medical-Devices-Data-Maintainer_R1280025",{"id":67,"name":68,"urlSafeSlug":68,"logo":69},[262],{"city":166,"region":167,"country":168},"2022-09-07T00:00:00Z","Candidates should possess a Bachelor of Science degree or related experience, along with good PC literacy skills, including Word and Excel, and the ability to carry out analysis and information gathering to resolve problems on routine matters. Developing knowledge of the company’s products and the pharmaceutical industry is also required.","The Life & Science Recent Graduate will be responsible for setting up and maintaining Global Medical Devices Product data, performing data research to gather information on product attributes, identifying and correcting inaccurate data, updating reference files and databases, producing files and outputs for specified processes, and responding to queries on reference data as needed.",{"employment":267,"compensation":269,"experience":270,"visaSponsorship":275,"location":276,"skills":277,"industries":286},{"type":268},{"id":111,"name":112,"description":18},{"minAnnualSalary":18,"maxAnnualSalary":18,"currency":18,"details":18},{"experienceLevels":271},[272],{"id":273,"name":274,"description":18},"e677de98-10ce-4da6-9a88-ef9be4395dfe","Entry Level & New Grad",{"type":48},{"type":107},[278,279,280,281,282,283,284,285],"Data Research","Data Analysis","Data Management","Microsoft Excel","Microsoft Word","Problem Solving","Information Gathering","Communication",[287,288,290,291],{"id":66,"name":65},{"id":139,"name":289},"Data Science",{"id":139,"name":140},{"id":139,"name":292},"Medical Devices",{"id":294,"title":295,"alternativeTitles":296,"slug":307,"jobPostId":294,"description":308,"applyUrl":309,"company":68,"companyOption":310,"locations":311,"listingDate":316,"listingSite":104,"isRemote":55,"requirements":317,"responsibilities":318,"status":107,"expiryDate":18,"summary":319},"46ac3716-f5da-4813-a69a-419ca278880c","Biostatisticien Senior FSP, Phase Tardive (Senior Biostatistician)",[297,298,299,300,301,302,303,304,305,306],"Senior Biostatistician Late Phase Clinical Trials","Lead Biostatistician Phase III Drug Development","Principal Biostatistician Statistical Analysis","Senior Statistical Programmer Clinical Trials","Biostatistics Lead Late Phase Studies","Senior Biostatistician SAS/R Clinical Research","Clinical Biostatistician Phase 2/3","Senior Biostatistician Regulatory Submissions","Biostatistical Analyst Senior Clinical Trials","Senior Biostatistician Data Analysis Clinical Development","biostatisticien-senior-fsp-phase-tardive-senior-biostatistician-46ac3716-f5da-4813-a69a-419ca278880c","### Position Overview\n\n* **Location Type:** Remote (United States or Canada)\n* **Employment Type:** Full-time\n* **Salary:** Not specified (Details in French Job Description)\n\nThe Senior Biostatistician will provide statistical support to Phase 2/3 drug development programs with efficacy and safety endpoints. This role offers the opportunity to work remotely and collaborate with leading pharmaceutical and biotechnology companies, contributing to the advancement of therapies.\n\n### Requirements\n\n* Experience as a Biostatistician\n* Strong statistical skills\n* Experience with SAS and/or R\n* Ability to collaborate with multidisciplinary project teams\n* Experience with clinical trial protocols and data analysis plans\n\n### Responsibilities\n\n* Collaborate with project teams to establish project timelines.\n* Provide statistical data to study synopsis and protocols.\n* Write or revise statistical sections of clinical trial protocols, consulting internal and external experts.\n* Write or revise statistical analysis plans, datasets, and TLF specifications.\n* Provide guidance and supervision to programmers in writing analysis dataset specifications and programming tables, lists, and figures.\n* Effectively manage internal and CRO project activities, including timelines, deliverables, and resource availability.\n* Collaborate with data management, statistical programming, and clinical development teams.\n* Utilize SAS and/or R for inferential statistical analyses and validation of key data derivations.\n* Support exploratory analyses and publications.\n* Contribute to clinical study reports and other regulatory documents (e.g., DSUR, documentation).\n\n### Additional Benefits\n\n* Remote work from home\n* Work-life balance and flexible hours\n* Collaboration with motivated and high-performing research and statistics teams\n* Technical training and personalized development program\n* Research opportunities aligned with unique skills\n* Promising career path\n* Job stability: long-term commitments and redeployment opportunities\n* Focus on bringing new therapies to market rather than project budgets and change orders\n* Regulatory submission experience\n* Engaging and fast-paced environment\n* Good work-life balance\n\n### Company Information\n\nData Sciences Staffing Solutions (DS3) is a unit of IQVIA providing fully integrated resources to sponsors through a Functional Service Provider (FSP) partnership. This allows employees to benefit from working for a leading global CRO while collaborating with sponsor teams and utilizing sponsor systems. Clients include leading pharmaceutical and biotechnology companies.","https://iqvia.wd1.myworkdayjobs.com/iqvia/job/Kirkland-Quebec-Canada/Biostatisticien-Senior-FSP--Phase-Tardive--Senior-Biostatistician-_R1457629",{"id":67,"name":68,"urlSafeSlug":68,"logo":69},[312],{"city":313,"region":314,"country":315},"Kirkland","Quebec","Canada","2025-03-26T00:00:00Z","Candidates should possess a Bachelor's degree in Biostatistics, Statistics, Mathematics, or a related field, and hold a Master's degree is preferred. They should have at least 7 years of experience in biostatistical analysis, particularly within clinical trials, with a strong understanding of statistical methods and SAS or R programming. Experience with Phase 2/3 drug development is highly desirable.","The Senior Biostatistician will collaborate with multidisciplinary project teams to establish project timelines, provide statistical data for studying clinical trial summaries and protocols, and draft or revise statistical sections of clinical trial protocols, consulting with internal and external experts. They will also draft or revise statistical analysis plans, datasets, and TLF specifications, offer guidance and supervision to programmers in developing analysis datasets and programming tables, lists, and figures, manage internal and CRO project activities, and support exploratory analyses and publications, contributing to clinical study reports and regulatory documents such as DSURs.",{"employment":320,"compensation":322,"experience":324,"visaSponsorship":327,"location":328,"skills":329,"industries":338},{"type":321},{"id":111,"name":112,"description":18},{"minAnnualSalary":18,"maxAnnualSalary":18,"currency":18,"details":323},"Salary not specified; details available in French job description",{"experienceLevels":325},[326],{"id":121,"name":122,"description":18},{"type":48},{"type":48},[330,331,332,333,334,335,336,337],"Biostatistics","SAS","R","Clinical trial protocols","Data analysis plans","Statistical analysis","Data management","Regulatory documentation",[339,340],{"id":139,"name":140},{"id":63,"name":62},{"id":342,"title":343,"alternativeTitles":344,"slug":355,"jobPostId":342,"description":356,"applyUrl":357,"company":68,"companyOption":358,"locations":359,"listingDate":361,"listingSite":104,"isRemote":55,"requirements":362,"responsibilities":363,"status":107,"expiryDate":18,"summary":364},"f5c3a080-430e-4ada-b173-ecfc2f587349","Biostatisticien Principal FSP, Pharmacocinétique (Principal Biostatistician)",[345,346,347,348,349,350,351,352,353,354],"Principal Biostatistician Pharmacokinetics","Senior Biostatistician PK/PD","Lead Biostatistician Clinical Trials","Biostatistician Neurosciences","Pharmacokinetic Biostatistician","Clinical Biostatistician PK","Biostatistical Lead Regulatory Submissions","Senior Statistical Programmer Pharmacokinetics","Biostatistician Drug Development PK","Principal Statistical Scientist PK","biostatisticien-principal-fsp-pharmacocinetique-principal-biostatistician-f5c3a080-430e-4ada-b173-ecfc2f587349","### Position Overview\n\n* **Location Type:** Remote (United States or Canada)\n* **Employment Type:** Full-time\n* **Job Title:** Principal Biostatistician - Phase I Clinical Development (PK)\n* **Company:** Data Sciences Staffing Solutions (DSSS), an IQVIA unit\n\n**Description:** The Principal Biostatistician is responsible for providing statistical support to new clinical research in neuroscience. This role offers opportunities to influence the future of medicine and advance therapies within a leading global CRO. You'll collaborate with interdisciplinary teams of sponsors.\n\n### Responsibilities\n\n* Collaborate with multidisciplinary project teams to establish project goals and timelines.\n* Draft statistical sections of clinical trial protocols, consulting with internal and external experts.\n* Develop statistical analysis plans.\n* Monitor internal and CRO project activities, including deadlines, deliverables, and resource availability.\n* Collaborate with data management, clinical development, and clinical operations with statistical expertise.\n* Contribute to clinical studies/statistical reports and other regulatory documents.\n* Provide guidance and supervision to programmers in writing data analysis set specifications and programming tables, lists, and figures.\n* Interpret study results and review study outcome reports for accuracy.\n* Support exploratory analyses and business medical publications.\n* Participate in other activities and meetings to support biostatistics and development team as needed.\n\n### Requirements\n\n* Experience with regulatory submissions. (Specific details are not provided)\n\n### Additional Benefits\n\n* Work-from-home opportunities\n* Work-life balance and flexible schedules\n* Technical training and customized development curriculum\n* Research opportunities aligned with unique skills\n* Promising career path\n* Job stability: long-term commitments and redeployment opportunities\n* Focus on marketing new treatments rather than project budgets and modifications.\n* Engaging and fast-paced environment\n* Good work-life balance\n\n### Company Information\n\nData Sciences Staffing Solutions (DSSS) is a unit of IQVIA, providing fully integrated resources to clients through a Functional Service Provider (FSP) partnership. DSSS partners with leading pharmaceutical and biotechnology companies, offering unique opportunities to influence the future of medicine and advance therapies.","https://iqvia.wd1.myworkdayjobs.com/iqvia/job/Kirkland-Quebec-Canada/Principal-Biostatisticain-FSP_R1453880",{"id":67,"name":68,"urlSafeSlug":68,"logo":69},[360],{"city":313,"region":314,"country":315},"2025-04-11T00:00:00Z","Candidates should possess a Master's degree in Biostatistics, Statistics, or a related field, and have a minimum of 8 years of experience in biostatistical analysis, with a strong focus on pharmacokinetic (PK) modeling and clinical development. Experience with regulatory submissions is required, and knowledge of neuroscientific research is highly desirable.","The Principal Biostatistician will collaborate with multidisciplinary project teams to establish project goals and timelines, draft statistical sections within clinical trial protocols, and develop statistical analysis plans. They will monitor project activities and CRO operations, collaborate with data management and clinical development teams, contribute to clinical studies and regulatory documents, provide statistical advice and supervision to programmers, interpret study results, support exploratory analyses and business medical publications, and participate in various activities to support biostatistical and development teams.",{"employment":365,"compensation":367,"experience":369,"visaSponsorship":372,"location":373,"skills":374,"industries":380},{"type":366},{"id":111,"name":112,"description":18},{"minAnnualSalary":18,"maxAnnualSalary":18,"currency":18,"details":368},"Not specified",{"experienceLevels":370},[371],{"id":121,"name":122,"description":18},{"type":48},{"type":48},[375,333,376,377,378,379],"Statistical support","Statistical analysis plans","Regulatory submissions","Data analysis","Programming (implied for data analysis and reporting)",[381,382,383],{"id":139,"name":140},{"id":63,"name":62},{"id":139,"name":384},"Clinical Research",{"id":386,"title":387,"alternativeTitles":388,"slug":404,"jobPostId":386,"description":405,"applyUrl":406,"company":68,"companyOption":407,"locations":408,"listingDate":412,"listingSite":104,"isRemote":55,"requirements":413,"responsibilities":414,"status":107,"expiryDate":18,"summary":415},"d8f565b8-f4a7-44fa-96ea-5cc1adda7b76","Field Service Technician",[389,390,391,392,393,394,395,396,397,398,399,400,401,402,403],"Medical Equipment Field Service Engineer","Biomedical Equipment Technician","Healthcare Automation Service Specialist","Clinical Engineering Field Technician","Electromechanical Service Technician (Healthcare)","Medical Device Repair Technician","Field Service Engineer - Medical Devices","Automation Technician - Healthcare","Hospital Equipment Maintenance Technician","Biomedical Field Service Engineer","Medical Systems Service Technician","Clinical Field Service Specialist","Healthcare Technology Field Support","Medical Device Field Engineer","Field Service Technician - Biomedical","field-service-technician-d8f565b8-f4a7-44fa-96ea-5cc1adda7b76","### Position Overview\n- **Location Type:** Onsite (Travel required locally)\n- **Job Type:** Part-time, On-Call, Field Service Technician\n- **Salary:** Not specified\n\nThis is a PART-TIME, On-Call, Field Service Technician opportunity with approximately 20-25 hours per week. You will have a flexible schedule and an opportunity to grow and expand into new opportunities while earning supplemental income and learning the medical device industry. The role involves troubleshooting, repairing, and updating medical devices in hospitals, pharmacies, and other clinical settings, primarily supporting an automated medication dispensing system. Hiring is happening ASAP.\n\n### Responsibilities\n- Troubleshoot and repair existing devices and document the activities correctly.\n- Hardware parts replacement, as well as software updates and calibrations.\n- Perform bi-annual or yearly preventative maintenance as determined by the customer.\n- Assist in the installation and implementation of new devices at customer locations.\n- Conduct routine system checks and record data from product tests after installation and configuration.\n- Maintain and stock parts and tools assigned by the customer.\n- Per-diem position requiring travel and flexibility to work with your current schedule.\n- Available on-call including nights and weekends.\n- Travel locally for up to 2-3 hours to support customer needs.\n- Respond to and arrive at customer sites within the service ticket’s Service Level Agreement (within 4 hours, 8 hours, 12 hours, or 24 hours per the details of each ticket).\n\n### Requirements\n- Intermediate troubleshooting abilities in the disciplines of electronics, mechanics, and electromechanical systems.\n- Experience as a military technician, computer technician, or other complex electronics technician preferred.\n- Experience supporting automation equipment in a healthcare setting is a plus.\n- A+ certification preferred.\n- Experience in healthcare, field service, engineering, biomedical, maintenance, customer service, pharmacy technician, electronics, electrical, technical work, or IT is beneficial.\n- Strong communication skills and ability to provide exceptional customer support.\n- Must have an active driver’s license and a personal vehicle to use for job-related assignments (travel time and mileage are reimbursed).\n- Ability to clear hospital vendor credentialing requirements, including proof of vaccination status, required.\n\n### Application Instructions\n- Create an account on the company website (takes less than one minute).\n- Complete the application, which takes approximately 5-7 minutes.\n\n### Company Information\n- **Company:** IQVIA\n- **Industry:** Healthcare (Medical Device Technology)","https://iqvia.wd1.myworkdayjobs.com/iqvia/job/Anchorage-AK/Field-Service-Technician_R1480515",{"id":67,"name":68,"urlSafeSlug":68,"logo":69},[409],{"city":410,"region":411,"country":24},"Anchorage","Alaska","2025-04-24T00:00:00Z","Candidates must have intermediate troubleshooting abilities in electronics, mechanics, and electromechanical systems, with preferred experience as a military technician, computer technician, or other complex electronics technician, and experience supporting automation equipment in a healthcare setting. An +A certification is preferred, and experience in healthcare, field service, engineering, biomedical, maintenance, customer service, pharmacy technician, electronics, electrical, technical work, or IT is beneficial. Applicants must possess a valid driver’s license and a personal vehicle, along with the ability to clear hospital vendor credentialing requirements, including proof of vaccination status.","The Field Service Technician will troubleshoot, repair, and update medical devices inside hospitals, pharmacies, and other clinical settings, performing hardware parts replacement, software updates, and calibrations. They will conduct bi-annual or yearly preventative maintenance, assist in the installation and implementation of new devices, perform routine system checks and record data, maintain and stock parts and tools, travel locally for up to 2-3 hours to support customer needs, respond to customer site requests within specified Service Level Agreements, and provide exceptional customer support.",{"employment":416,"compensation":419,"experience":421,"visaSponsorship":424,"location":425,"skills":426,"industries":439},{"type":417},{"id":273,"name":418,"description":18},"Part Time",{"minAnnualSalary":18,"maxAnnualSalary":18,"currency":18,"details":420},"Part-time, on-call position with supplemental income.",{"experienceLevels":422},[423],{"id":121,"name":122,"description":18},{"type":48},{"type":107},[427,428,429,430,431,432,433,434,435,436,437,438],"Troubleshooting","Electronics","Mechanics","Electromechanical Systems","Hardware Repair","Software Updates","Calibration","Preventative Maintenance","Installation","Biomedical","Field Service","A+ Certification",[440,442],{"id":139,"name":441},"Medical Device",{"id":66,"name":65},{"id":444,"title":445,"alternativeTitles":446,"slug":462,"jobPostId":444,"description":463,"applyUrl":464,"company":68,"companyOption":465,"locations":466,"listingDate":471,"listingSite":104,"isRemote":55,"requirements":472,"responsibilities":473,"status":107,"expiryDate":18,"summary":474},"38e0a3db-8a0d-46cc-b77f-1f07ee7a24bb","Senior Software Developer (w/m/d) HealthTec",[447,448,449,450,451,452,453,454,455,456,457,458,459,460,461],"Senior Java Developer HealthTech","Senior JavaScript Developer HealthTech","Lead Software Engineer HealthTech","Senior Full Stack Developer HealthTech","Senior Backend Developer HealthTech","Senior Frontend Developer HealthTech","HealthTech Software Architect","Senior Java Backend Developer HealthTech","Senior JavaScript Frontend Developer HealthTech","Agile Software Developer HealthTech","Senior IT Solutions Developer HealthTech","Senior Digital Health Software Engineer","Senior Healthcare Software Developer","Senior Java/JavaScript Developer HealthTech","Senior Software Engineer (Digital Health)","senior-software-developer-w-m-d-healthtec-38e0a3db-8a0d-46cc-b77f-1f07ee7a24bb","### Position Overview\n- **Location Type:** Onsite (with Remote Option)\n- **Employment Type:** Full-time (or Part-time – 35+ hours/week)\n- **Salary:** Not specified\n\nDAVASO is a leading technology provider and service provider in the German healthcare market. Our activities focus on permitting and billing management, software development and deployment, and digitalization and archiving services for health insurance companies. Founded in Leipzig in 1990, DAVASO is now one of the largest employers in the Leipzig region, with over 1,300 dedicated and competent employees. Since 2021, we have been part of the IQVIA Group. We are looking for you for our business unit in Dortmund with approximately 170 employees. For our customers in the healthcare sector, we develop software for the digitalization of business processes from architecture to implementation. We rely on standard technologies, but also keep an eye on new developments. You will work in the dynamic environment of an IT company with current technologies and IT systems.\n\n### Responsibilities\n- Design and implementation of software products in customer projects\n- Creation of concepts and documentation\n- Optimization of efficient and innovative solutions for the processing of digital processes\n- Further development of existing solutions with customer-specific adaptations\n- Application of agile Scrum and Kanban methods\n- Development of ideas for our processes and software products\n\n### Requirements\n- Successfully completed studies in (Business) Informatics or a vocational training as an IT specialist (application development) or equivalent IT training\n- Several years of professional experience in software development\n- Programming experience with Java and JavaScript, with an interest in innovative technologies\n- Responsibility and a structured approach to work\n- Basic knowledge of business processes in companies\n- Knowledge of common relational databases\n- Fluent written and spoken German (B2/C1)\n- Good English skills\n\n### Application Instructions\n- Not specified\n\n### Company Information\nIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization.","https://iqvia.wd1.myworkdayjobs.com/iqvia/job/Dortmund-Germany/Senior-Software-Developer--w-m-d--HealthTec_R1471443",{"id":67,"name":68,"urlSafeSlug":68,"logo":69},[467],{"city":468,"region":469,"country":470},"Dortmund","North Rhine-Westphalia","Germany","2025-05-14T00:00:00Z","Candidates should possess a completed degree in computer science or a related field, or an equivalent IT qualification, and have several years of professional experience in software development. They should be proficient in Java and JavaScript programming, demonstrate an interest in innovative technologies, and possess fundamental knowledge of business processes within organizations. Strong knowledge of relational databases is also required, along with fluent German language skills (B2/C1 level) and basic English language skills.","The Senior Software Developer will be responsible for designing and implementing software products within customer projects, creating concepts and documentation, optimizing efficient and innovative solutions for digital process handling, and further developing existing solutions with customer-specific adaptations. They will also apply agile Scrum and Kanban methodologies, develop ideas for processes and software products, and contribute to the overall development of the company's processes and software products.",{"employment":475,"compensation":477,"experience":478,"visaSponsorship":482,"location":483,"skills":485,"industries":492},{"type":476},{"id":111,"name":112,"description":18},{"minAnnualSalary":18,"maxAnnualSalary":18,"currency":18,"details":18},{"experienceLevels":479},[480,481],{"id":234,"name":235,"description":18},{"id":179,"name":180,"description":18},{"type":48},{"type":484},4,[486,128,487,488,489,490,491],"Java","Relational Databases","German (B2/C1)","Agile Scrum","Kanban","Software Development",[493,494],{"id":66,"name":65},{"id":139,"name":495},"Information Technology",{"id":497,"title":498,"alternativeTitles":499,"slug":514,"jobPostId":497,"description":515,"applyUrl":516,"company":68,"companyOption":517,"locations":518,"listingDate":471,"listingSite":104,"isRemote":55,"requirements":523,"responsibilities":524,"status":107,"expiryDate":18,"summary":525},"e192d783-bfb8-4c24-a0e7-53a7e1fcfbca","2076 - Accountant 3",[500,501,502,503,504,505,506,507,508,509,510,511,512,513],"Senior Accountant","General Ledger Accountant","Financial Accountant","Staff Accountant","Corporate Accountant","Reconciliation Accountant","Accounting Specialist","Financial Reporting Accountant","Accounts Specialist","Certified Public Accountant (CPA) Candidate","Public Accountant","Commercial Accountant","Fiscal Accountant","Certified Public Accountant (CPA)","2076-accountant-3-e192d783-bfb8-4c24-a0e7-53a7e1fcfbca","### Position Overview\n- **Location Type:** Hybrid\n- **Job Type:** Full time\n- **Salary:** Not specified\n- **Location:** Warsaw, Poland\n- **Company:** IQVIA\n\nIQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. With approximately 88,000 employees, IQVIA conducts operations in more than 100 countries. IQVIA creates intelligent connections across all aspects of healthcare through its analytics, transformative technology, big data resources and extensive domain expertise. In such way we support our clients enabling customers to accelerate the clinical development and commercialization of innovative medical treatments that improve healthcare outcomes for patients.\n\nAre you ready to move Healthcare forward? Start your career at IQVIA!\n\nTo learn more, visit [www.iqvia.com](www.iqvia.com).\n\n### Requirements\n- **Education:** Bachelor’s Degree\n- **Experience:** 3 years experience in accounting\n- **Software Knowledge:**\n - Knowledge of PeopleSoft Finance modules\n - Proficiency in Microsoft Office applications (Word, Excel, etc.)\n- **Skills:**\n - Technical accounting skills\n - Good analytical and numeracy skills\n - Ability to exercise judgment within procedures and practices\n - Ability to prioritize and coordinate multiple work requirements\n - Ability to establish and maintain effective working relationships\n\n### Responsibilities\n- Recommend, develop, implement and / or maintain standards for functional roles.\n- Analyze, prepare and process journal entries.\n- Analyze, maintain and reconcile general ledger accounts.\n- Provide records of assets, liabilities and other financial transactions.\n- Prepare profit and loss, income and balance sheet statements.\n- Maintain inter-company accounting records and reconciliations.\n- Prepare ad hoc reports for internal and inter-departmental use.\n- Prepare reports and analyze for use in the annual external audit.\n- Ensure accuracy and compliance with all accounting regulations and Sarbanes Oxley requirements.\n- Check that appropriate approvals are obtained for accounting purposes.\n- Provide recommendations to improve existing processes and suggest alternatives where appropriate.\n- Prepare monthly bank account reconciliations.\n- Maintain receipts and disbursement reports.\n- Interpret reports and records for managers.\n- Perform other duties as assigned.\n\n### Application Instructions\n- Not specified in the provided job description. Interested candidates should visit [www.iqvia.com](www.iqvia.com) for more information on how to apply.","https://iqvia.wd1.myworkdayjobs.com/iqvia/job/Warsaw-Poland/XMLNAME-2076---Accountant-3_R1456819",{"id":67,"name":68,"urlSafeSlug":68,"logo":69},[519],{"city":520,"region":521,"country":522},"Warsaw","Masovian Voivodeship","Poland","Candidates must possess a Bachelor’s degree and a minimum of 3 years of experience in accounting, along with knowledge of PeopleSoft Finance modules and proficiency in Microsoft Office applications. Strong technical accounting skills, analytical and numeracy abilities, and the capacity to exercise sound judgment within established procedures are also required, alongside the ability to prioritize and coordinate multiple work requirements and establish effective working relationships.","The Accountant 3 will recommend, develop, implement, and maintain accounting standards, analyze and prepare journal entries, maintain and reconcile general ledger accounts, provide records of financial transactions, prepare financial statements, maintain inter-company accounting records, prepare ad hoc reports, ensure accuracy and compliance with accounting regulations and Sarbanes Oxley requirements, check for appropriate approvals, provide recommendations for process improvements, prepare monthly bank account reconciliations, maintain receipts and disbursement reports, interpret reports for managers, and perform other duties as assigned.",{"employment":526,"compensation":528,"experience":530,"visaSponsorship":533,"location":534,"skills":535,"industries":544},{"type":527},{"id":111,"name":112,"description":18},{"minAnnualSalary":18,"maxAnnualSalary":18,"currency":529,"details":18},"USD",{"experienceLevels":531},[532],{"id":234,"name":235,"description":18},{"type":48},{"type":48},[536,537,538,539,540,541,542,543],"PeopleSoft Finance","Microsoft Office","Journal Entries","General Ledger","Financial Statements","Bank Reconciliation","Sarbanes Oxley","Accounting Standards",[545,547],{"id":139,"name":546},"Accounting",{"id":139,"name":548},"Finance",{"id":550,"title":551,"alternativeTitles":552,"slug":563,"jobPostId":550,"description":564,"applyUrl":565,"company":68,"companyOption":566,"locations":567,"listingDate":471,"listingSite":104,"isRemote":55,"requirements":572,"responsibilities":573,"status":107,"expiryDate":18,"summary":574},"f0a45c5a-9fc0-43aa-9c1e-751957a603eb","Informatore Scientifico del Farmaco (Genova)",[553,554,555,556,557,558,559,560,561,562],"Pharmaceutical Sales Representative Genoa","Medical Science Liaison Genoa","Drug Representative Genoa","Pharmaceutical Sales Specialist Genoa","Medical Representative Genoa","Gastroenterology Pharmaceutical Sales Genoa","General Practitioner Pharmaceutical Sales Genoa","ISF Freelance Genoa","Pharmaceutical Promoter Genoa","Medical Sales Executive Genoa","informatore-scientifico-del-farmaco-genova-f0a45c5a-9fc0-43aa-9c1e-751957a603eb","### Position Overview\n\n* **Location Type:** Onsite (Genova)\n* **Job Type:** Full Time\n* **Company:** IQVIA\n\nIQVIA, a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries, is seeking Medical Science Information Specialists (ISF) to join a significant project in the Genoa area. The ISF Freelance will be integrated into a major project managed directly by IQVIA, focusing on the promotion of a new pharmaceutical product and supplements to the target audience of general practitioners and gastroenterologists. Reporting directly to the Area Manager, the candidate will manage and maintain relationships with MMGs within their area of responsibility and collaborate with colleagues to achieve established goals.\n\n### Requirements\n\n* **Education:** Bachelor’s degree in scientific disciplines (Law 219/06)\n* **Experience:**\n * Experience in pharmaceutical promotion to General Practitioners or gastroenterologists.\n * Minimum six months of experience in a similar role within a structured organization.\n * Proven track record of achieving individual goals.\n\n### Responsibilities\n\n* Manage and maintain relationships with MMGs within assigned territory.\n* Collaborate with colleagues to achieve project goals.\n* Promote a new pharmaceutical product and supplements to the target audience.\n* Report to the Area Manager.\n\n### Application Instructions\n\n* **Candidature:** Candidatures without meeting the required criteria will not be considered.\n* **Data Consent:** Please include authorization to process personal data in accordance with Art. 13 of D.Lgs. 30 June 2003 n°196 – “Code on the protection of personal data” and Art. 13 GDPR 679/16 – “European regulation on the protection of personal data”.\n\n### Company Information\n\nIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at [https://jobs.iqvia.com](https://jobs.iqvia.com)\n\n#LI-CES #LI_DNPI","https://iqvia.wd1.myworkdayjobs.com/iqvia/job/Milan-Italy/Informatore-Scientifico-del-Farmaco--Genova-_R1484241",{"id":67,"name":68,"urlSafeSlug":68,"logo":69},[568],{"city":569,"region":570,"country":571},"Milan","Lombardy","Italy","The candidate should possess a Bachelor's degree in scientific disciplines (Law 219/06), experience in promoting pharmaceuticals to General Practitioners or gastroenterologists, and at least six months of experience in the same role at a structured company. A proven track record of achieving individual goals is also required.","The Informatore Scientifico del Farmaco (ISF) Freelance will manage and maintain relationships with MMG doctors in their area of expertise, collaborating with colleagues to achieve predefined objectives. They will also promote a launching drug and supplements within the target audience of general practitioners and gastroenterologists, reporting directly to the Area Manager.",{"employment":575,"compensation":577,"experience":578,"visaSponsorship":581,"location":582,"skills":583,"industries":590},{"type":576},{"id":111,"name":112,"description":18},{"minAnnualSalary":18,"maxAnnualSalary":18,"currency":18,"details":18},{"experienceLevels":579},[580],{"id":121,"name":122,"description":18},{"type":48},{"type":484},[584,585,586,587,588,589],"Pharmaceutical Promotion","General Practitioners","Gastroenterologists","Relationship Management","Sales","Achieving Goals",[591],{"id":139,"name":140},{"id":593,"title":594,"alternativeTitles":595,"slug":606,"jobPostId":593,"description":607,"applyUrl":608,"company":68,"companyOption":609,"locations":610,"listingDate":471,"listingSite":104,"isRemote":55,"requirements":613,"responsibilities":614,"status":107,"expiryDate":18,"summary":615},"c1cca45a-1e09-4205-ab57-0e270c0dec0b","Facilities Lead",[596,597,598,599,600,601,602,603,604,605],"Facilities Coordinator","Facilities Assistant Manager","Office Facilities Manager","Facilities Operations Lead","Building Operations Coordinator","Facilities Support Specialist","Facilities Administrator","Facilities Operations Assistant","Facilities Management Coordinator","Senior Facilities Assistant","facilities-lead-c1cca45a-1e09-4205-ab57-0e270c0dec0b","### Position Overview\n- **Location Type:** [Not Specified]\n- **Job Type:** Full Time\n- **Salary:** [Not Specified]\nAssists with daily tasks relating to facilities and office services as required.\n\n### Essential Functions\n- Ensure recycling program is carried out in a timely manner (under guidance).\n- Assist with internal office moves (under guidance and with direction).\n- Assist in completing facility-related requests from clients.\n- Inform management of problems relating to facility and office service issues.\n- Place calls for fax and copy machine maintenance as directed.\n- May interact with vendors, Accounts Receivable, Purchasing and other departments to research incorrect invoices and to code invoices.\n- May act as back-up for receptionist when requested.\n- Other duties as assigned by Manager.\n\n### Requirements\n- **Minimum Diploma**\n- **Minimum 2 years experience** in facility management.\n\n### Company Information\nIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. \nLearn more at: [https://jobs.iqvia.com](https://jobs.iqvia.com)","https://iqvia.wd1.myworkdayjobs.com/iqvia/job/Singapore/Facilities-Lead_R1483779",{"id":67,"name":68,"urlSafeSlug":68,"logo":69},[611],{"city":18,"region":18,"country":612},"Singapore","The ideal candidate should possess a minimum of two years of experience in facility management, along with a minimum diploma level of education. Experience working within the life sciences or healthcare industries is preferred, and familiarity with IQVIA’s operations would be beneficial.","As a Facilities Lead, you will assist with daily tasks related to facilities and office services, ensuring the recycling program is carried out, supporting internal office moves, and completing facility-related requests from clients. You will also inform management of facility and office service issues, place maintenance calls, and potentially interact with vendors and other departments to resolve invoice discrepancies. Additionally, you may act as a back-up for the receptionist and perform other duties as assigned by the Manager.",{"employment":616,"compensation":618,"experience":619,"visaSponsorship":622,"location":623,"skills":624,"industries":631},{"type":617},{"id":111,"name":112,"description":18},{"minAnnualSalary":18,"maxAnnualSalary":18,"currency":18,"details":18},{"experienceLevels":620},[621],{"id":121,"name":122,"description":18},{"type":48},{"type":48},[625,626,627,628,629,630],"Facility Management","Recycling Programs","Office Moves","Maintenance Calls","Vendor Management","Invoice Discrepancy Resolution",[632,633],{"id":66,"name":65},{"id":139,"name":140},{"id":635,"title":636,"alternativeTitles":637,"slug":648,"jobPostId":635,"description":649,"applyUrl":650,"company":68,"companyOption":651,"locations":652,"listingDate":471,"listingSite":104,"isRemote":55,"requirements":657,"responsibilities":658,"status":107,"expiryDate":18,"summary":659},"eba955f2-710f-4e8f-8602-874d24d1723a","Associate Market Access Specialist - Bulgaria",[638,639,640,641,642,643,644,645,646,647],"Market Access Specialist Bulgaria","Pharmaceutical Market Access Associate Bulgaria","Healthcare Access Specialist Bulgaria","Therapeutic Consultant Bulgaria","Stroke Care Market Access Specialist","Neuroscience Market Access Associate","Hospital Outreach Specialist Bulgaria","Clinical Access Manager Bulgaria","Market Access Manager Pharmaceutical Bulgaria","Regional Market Access Specialist Bulgaria","associate-market-access-specialist-bulgaria-eba955f2-710f-4e8f-8602-874d24d1723a","### Position Overview\n\n- **Location Type:** Onsite (Bulgaria)\n- **Employment Type:** Full-time\n- **Salary:** Not specified\n\nJoin the Angels Initiative Team! Every 30 minutes, a stroke patient who could have been saved dies or is permanently disabled because they were treated in the wrong hospital. Our mission is simple: to increase the number of patients treated in stroke-ready hospitals and to optimize the quality of treatment in all existing stroke centers. We are building a global community of stroke centers and stroke-ready hospitals, working every day to improve the quality of treatment for every stroke patient. This is a unique opportunity to join IQVIA in partnership with Boehringer Ingelheim to improve stroke care worldwide through a corporate social responsibility project. We are looking for an Angels Consultant based in Bulgaria who will join an exciting working environment in a dynamic and international atmosphere.\n\n### Responsibilities\n\n* Increase efficiency in the management of stroke patients.\n* Support hospitals and healthcare professionals with continuous training and organizational tools.\n* Serve as an expert Therapeutic Consultant, promoting new diagnostic and treatment guidelines to hospitals.\n* Foster and promote quality monitoring programs to maintain consistent hospital performance.\n* Expand the project’s reach to new hospitals.\n* Lead multidisciplinary stroke teams through continuous improvement.\n* Enhance therapeutic protocols in major hospitals.\n\n### Requirements\n\n* Proven experience in pharmaceutical sales (preferably related to neuroscience or stroke care).\n* Excellent scientific background.\n* A PhD in Neuroscience or a related field is desirable, but not required.\n* Strong interpersonal skills and high motivation.\n* Fluency in English (Bulgarian language fluency is required).\n* Leadership abilities.\n* Proactivity, flexibility, and problem-solving skills.\n* Valid driving license and willingness to travel up to 70% of the time.\n\n### Company Information\n\nIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.\n\nLearn more at: [https://jobs.iqvia.com](https://jobs.iqvia.com)\n\n#LI-CES #LI-CS1","https://iqvia.wd1.myworkdayjobs.com/iqvia/job/Sofia-Bulgaria/Associate-Market-Access-Specialist---Bulgaria_R1474549",{"id":67,"name":68,"urlSafeSlug":68,"logo":69},[653],{"city":654,"region":655,"country":656},"Sofia","Sofia City Province","Bulgaria","Candidates should possess proven experience in pharmaceutical sales, preferably related to neuroscience or stroke care, and a strong scientific background. A PhD in Neuroscience or a related field is desirable, but not required. Fluency in English is essential, with Bulgarian language fluency being required, and a valid driving license along with a willingness to travel up to 70% of the time is needed.","The Associate Market Access Specialist will increase efficiency in the management of stroke patients, support hospitals and healthcare professionals with continuous training and organizational tools, serve as an expert Therapeutic Consultant promoting new diagnostic and treatment guidelines, foster and promote quality monitoring programs, expand the project’s reach to new hospitals, lead multidisciplinary stroke teams through continuous improvement, and enhance therapeutic protocols in major hospitals.",{"employment":660,"compensation":662,"experience":663,"visaSponsorship":666,"location":667,"skills":668,"industries":679},{"type":661},{"id":111,"name":112,"description":18},{"minAnnualSalary":18,"maxAnnualSalary":18,"currency":18,"details":18},{"experienceLevels":664},[665],{"id":121,"name":122,"description":18},{"type":48},{"type":484},[669,670,671,672,673,674,675,676,677,678],"Pharmaceutical Sales","Neuroscience","Stroke Care","Scientific Background","English","Bulgarian","Therapeutic Consulting","Training","Quality Monitoring","Multidisciplinary Teams",[680,681],{"id":139,"name":140},{"id":66,"name":65},{"id":683,"title":684,"alternativeTitles":685,"slug":701,"jobPostId":683,"description":702,"applyUrl":703,"company":68,"companyOption":704,"locations":705,"listingDate":710,"listingSite":104,"isRemote":55,"requirements":711,"responsibilities":712,"status":107,"expiryDate":18,"summary":713},"266e6b5f-1ee2-4e2a-a60a-92690760f091","Clinical Research Associate, Multi-Sponsor, France",[686,687,688,689,690,691,692,693,694,695,696,697,698,699,700],"Clinical Research Monitor, France","Clinical Trial Monitor, Multi-Sponsor","Field Clinical Research Associate, France","On-Site Clinical Research Coordinator, France","Clinical Study Monitor, Multi-Sponsor","GCP Clinical Research Associate, France","Clinical Research Auditor, France","Site Monitoring Specialist, Clinical Trials","Clinical Operations Associate, France","Multi-Site Clinical Research Associate","Clinical Research Field Monitor, France","Clinical Trial Site Manager, France","Clinical Research Project Monitor","Clinical Research Associate - Site Management","Clinical Research Associate - GCP Compliance","clinical-research-associate-multi-sponsor-france-266e6b5f-1ee2-4e2a-a60a-92690760f091","### Position Overview\n- **Location Type:** [Location Type - Not specified]\n- **Employment Type:** Full Time\n- **Job Type:** Training Program\n\n**Job Description:** Engage in a structured training program to gain knowledge and skills required to independently conduct clinical monitoring visits in accordance with study protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements.\n\n### Essential Functions\n- Complete appropriate therapeutic, protocol, and clinical research training to perform job duties.\n- Gain experience in study procedures by working with experienced clinical staff.\n- Under close supervision, perform site monitoring visits (selection, initiation, monitoring, and close-out visits) in accordance with contracted scope of work and good clinical practices.\n- Under close supervision, administer protocol and related study training to assigned sites and establishes regular lines of communication with sites to manage ongoing project expectations and issues.\n- Under close supervision, evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate.\n- Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, Case Report Form (CRF) completion and submission, and data query generation and resolution.\n- Under close supervision, ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator’s Site File (ISF) is maintained in accordance with Good Clinical Practice (GCP) / International Conference on Harmonization (ICH) and local regulatory requirements.\n- Under close supervision, may support start-up phase.\n- Under close supervision, create and maintain appropriate documentation regarding site management, monitoring visit findings, and action plans by submitting regular visit reports, generating follow-up letters, and other required study documentation.\n- Collaborate and liaise with study team members for project execution support as appropriate.\n- If applicable, learn key facets for successful development of project subject recruitment plan on a per site basis. Suggest ideas for improving site recruitment plan in line with project needs to enhance predictability. Assist in tracking subject site recruitment progress.\n\n### Qualifications\n- **Education:** Bachelor’s Degree in a scientific discipline or health care preferred. (Equivalent combination of education, training, and experience may be accepted in lieu of a degree.)\n- **Experience:** Prior clinical experience preferred. (Some organizations may require 2 years of clinical experience.)\n- **Technical Skills:**\n - Computer skills including proficiency in Microsoft Word, Excel, and PowerPoint.\n - Proficiency in using a laptop computer, iPhone, and iPad (where applicable).\n- **Communication Skills:** Written and verbal communication skills, including good command of the English language.\n- **Soft Skills:** Organizational and problem-solving skills, effective time and financial management skills, and the ability to establish and maintain relationships.\n\n### Application Instructions\n- [Not specified - Requires additional information]\n\n### Company Information\n- [Not specified - Requires additional information]","https://iqvia.wd1.myworkdayjobs.com/iqvia/job/Paris-France/Clinical-Research-Associate--Multi-Sponsor--France_R1484304",{"id":67,"name":68,"urlSafeSlug":68,"logo":69},[706],{"city":707,"region":708,"country":709},"Paris","Île-de-France","France","2025-05-15T00:00:00Z","Candidates should possess a Bachelor's degree in a scientific discipline or healthcare field, which is preferred; equivalent combinations of education, training, and experience may be accepted in lieu of a degree; prior clinical experience is preferred, potentially requiring up to 2 years; proficiency in Microsoft Word, Excel, and PowerPoint, along with the ability to use a laptop computer, iPhone, and iPad is necessary; strong written and verbal communication skills, including a good command of the English language are required; effective organizational and problem-solving skills, as well as time and financial management skills are needed; and the ability to establish and maintain effective working relationships is essential.","The Clinical Research Associate will complete training to independently conduct clinical monitoring visits, perform site monitoring visits in accordance with study protocol and good clinical practice, administer protocol training to sites, evaluate site practices, manage study progress by tracking regulatory submissions and data queries, ensure availability of study documents, create and maintain documentation regarding site management, submit regular visit reports, and collaborate with study team members for project execution support. They may also support the start-up phase, contribute to subject recruitment plans, and track recruitment progress.",{"employment":714,"compensation":716,"experience":718,"visaSponsorship":722,"location":723,"skills":724,"industries":738},{"type":715},{"id":111,"name":112,"description":18},{"minAnnualSalary":18,"maxAnnualSalary":18,"currency":529,"details":717},"Base salary with potential bonuses.",{"experienceLevels":719},[720,721],{"id":121,"name":122,"description":18},{"id":273,"name":274,"description":18},{"type":48},{"type":48},[725,726,727,728,282,281,729,730,731,732,733,734,735,736,737,587],"Clinical Monitoring","Site Monitoring","Study Protocol","Good Clinical Practice","Microsoft PowerPoint","Data Queries","Regulatory Submissions","Documentation","Communication (Written)","Communication (Verbal)","Time Management","Financial Management","Problem-Solving",[739,740],{"id":139,"name":140},{"id":139,"name":384},{"id":742,"title":743,"alternativeTitles":744,"slug":760,"jobPostId":742,"description":761,"applyUrl":762,"company":68,"companyOption":763,"locations":764,"listingDate":710,"listingSite":104,"isRemote":55,"requirements":768,"responsibilities":769,"status":107,"expiryDate":18,"summary":770},"191fa3a7-2add-429c-96f0-c1ae7c91acf7","Pharmacovigilance Specialist/ IQVIA Services",[745,746,747,748,749,750,751,752,753,754,755,756,757,758,759],"Pharmacovigilance Associate IQVIA","Drug Safety Specialist IQVIA","Pharmacovigilance Case Processor IQVIA","Pharmacovigilance Data Entry Specialist IQVIA","Pharmacovigilance Quality Control Specialist IQVIA","Pharmacovigilance Reporting Specialist IQVIA","Pharmacovigilance Operations Specialist IQVIA","Pharmacovigilance Analyst IQVIA","Drug Safety Case Manager IQVIA","Pharmacovigilance Compliance Specialist IQVIA","Pharmacovigilance Medical Information Specialist IQVIA","Pharmacovigilance Regulatory Affairs Specialist IQVIA","Pharmacovigilance Safety Data Specialist IQVIA","Pharmacovigilance Literature Reviewer IQVIA","Pharmacovigilance Signal Detection Specialist IQVIA","pharmacovigilance-specialist-iqvia-services-191fa3a7-2add-429c-96f0-c1ae7c91acf7","### Position Overview\n\n* **Location Type:** Flexible Style Work (Remote base with occasional office visits)\n* **Employment Type:** Full-time\n* **Salary:** Not specified\n\nThis position involves safety information management related to pharmaceuticals and medical devices, encompassing activities from receiving and triaging safety data to preparing reports for regulatory agencies. The role requires meticulous attention to detail and strong communication skills.\n\n### Requirements\n\n* **Minimum Experience:** 3+ years of experience in safety information case processing (receiving, triaging, numbering, content verification, database entry/QC). Limited experience may be considered on a case-by-case basis.\n* **Language Proficiency:** Business-level Japanese language skills.\n* **Education:** High school diploma or higher (Associate's Degree, Bachelor's Degree, or Vocational School Diploma preferred).\n* **Interpersonal Skills:** Ability to build good relationships with other departments and team members.\n\n### Responsibilities\n\n* Receive, triage, number, and verify safety information.\n* Input safety information into a database and perform quality control (QC).\n* Perform initial assessment of PMDA reporting requirements.\n* Prepare and QC English explanation of cases (日英).\n* Create and QC reports for PMDA.\n* Conduct follow-up investigations (queries) to gather additional information.\n* Detect and evaluate safety-related information from domestic and international literature and overseas measures.\n* Input and QC safety-related information into a database, create reports for PMDA, and report to partnering companies.\n* Analyze case collections, detect and evaluate signals, and prepare reports.\n* Create draft reports for safety regular reports, infection disease regular reports, unsolicited adverse drug reaction regular reports, and clinical trial annual reports.\n* Prepare and QC reports for regulatory agencies and partner companies.\n* Create line lists for clinical trial facilities.\n\n### Company Information\n\nIQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.\n\nLearn more at: [https://jobs.iqvia.com](https://jobs.iqvia.com)","https://iqvia.wd1.myworkdayjobs.com/iqvia/job/Tokyo-Japan/Pharmacovigilance-Specialist--IQVIA-Services_R1484389",{"id":67,"name":68,"urlSafeSlug":68,"logo":69},[765],{"city":18,"region":766,"country":767},"Tokyo","Japan","Candidates must possess at least 3 years of experience in safety information case processing, including receipt, triage, numbering, content verification, database input, and QC. They should also have a business-level understanding of Japanese, a higher education degree (such as associate's or bachelor's), and the ability to build positive relationships with other departments and team members.","The Pharmacovigilance Specialist will be responsible for receiving and triaging safety information, assigning numbering, performing content verification, inputting data into databases, conducting initial assessments for PMDA reports, and performing QC. They will also create and QC explanation texts (in both Japanese and English), prepare and QC reports for submission to the PMDA, conduct investigations (queries) to obtain additional information, detect and evaluate signals from domestic and international literature and overseas measures, input data into databases and QC, and create reports for submission to PMDA. Additionally, the role involves preparing draft safety reports, infection reports, and annual reports, as well as creating line lists for clinical trial sites, and collaborating with various stakeholders including customers and clinical trial facilities.",{"employment":771,"compensation":773,"experience":775,"visaSponsorship":779,"location":780,"skills":781,"industries":794},{"type":772},{"id":111,"name":112,"description":18},{"minAnnualSalary":18,"maxAnnualSalary":18,"currency":529,"details":774},"Base salary",{"experienceLevels":776},[777,778],{"id":234,"name":235,"description":18},{"id":121,"name":122,"description":18},{"type":48},{"type":48},[782,783,784,785,786,787,788,789,790,791,792,793],"Safety Information Case Processing","Triage","Numbering","Content Verification","Database Input","QC","PMDA Reports","Japanese (Business Level)","Report Writing","Signal Detection","Data Input","Line Lists",[795,796],{"id":139,"name":200},{"id":139,"name":292},{"id":798,"title":799,"alternativeTitles":800,"slug":816,"jobPostId":798,"description":817,"applyUrl":818,"company":68,"companyOption":819,"locations":820,"listingDate":710,"listingSite":104,"isRemote":55,"requirements":824,"responsibilities":825,"status":107,"expiryDate":18,"summary":826},"6e585173-01f7-4619-b7fe-42ed38b57ac4","Clinical Research Associate, Multi-Sponsor, Belgium",[801,802,803,804,805,806,807,808,809,810,811,812,813,814,815],"Clinical Research Associate Belgium","CRA Belgium","Clinical Trial Monitor Belgium","On-Site Clinical Research Associate Belgium","Clinical Research Monitor Belgium","Clinical Study Monitor Belgium","Field Clinical Research Associate Belgium","Clinical Research Specialist Belgium","Clinical Trials Associate Belgium","Pharmaceutical Clinical Research Associate Belgium","Biotech Clinical Research Associate Belgium","Medical Device Clinical Research Associate Belgium","Clinical Research Coordinator Belgium","Clinical Project Associate Belgium","Clinical Research Auditor Belgium","clinical-research-associate-multi-sponsor-belgium-6e585173-01f7-4619-b7fe-42ed38b57ac4","### Position Overview\n- **Location Type:** Belgium based\n- **Job Type:** Full Time\n- **Salary:** (Salary not provided in the text)\nIQVIA Belgium is seeking a talented and motivated Clinical Research Associate (CRA) to join our Site Management team (Junior - Senior). This role offers an excellent opportunity to gain experience in diverse therapeutic areas and build a strong career within the organization.\n\n### Requirements\n- University degree in a scientific discipline or healthcare field.\n- Experience in the Pharma Industry and/or Clinical Trials environment.\n- Very good computer skills, including MS Office.\n- Excellent command of Dutch, French, and English languages.\n- Driver’s license class B (if applicable).\n\n### Responsibilities\n- Perform site monitoring visits (selection, initiation, monitoring, and close-out visits) in accordance with contracted scope of work and regulatory requirements (GCP and ICH guidelines).\n- Work with sites to adapt, drive, and track subject recruitment plans to enhance predictability.\n- Administer protocol and related study training to assigned sites and establish regular communication with sites to manage ongoing project expectations and issues.\n- Evaluate the quality and integrity of study site practices related to protocol conduct and regulatory adherence. Escalate quality issues as appropriate.\n- Manage the progress of assigned studies by tracking regulatory submissions, recruitment, enrollment, CRF completion, and data query resolution.\n- Ensure copies/originals of site documents are available for the Trial Master File (TMF) and verify the Investigator’s Site File (ISF) is maintained according to GCP and local regulatory requirements.\n- Create and maintain documentation regarding site management, monitoring visit findings, and action plans through visit reports, follow-up letters, and other required study documentation.\n- Collaborate with study team members for project execution support.\n- (Potentially) Support the development of project subject recruitment plans on a per-site basis.\n- (Potentially) Manage site financial management according to the clinical trial agreement and retrieve invoices according to local requirements.\n\n### Application Instructions\n- (Application instructions not provided in the text)\n\n### Company Information\n- **Company:** IQVIA Belgium\n- **Department:** Site Management\n- **Role:** Clinical Research Associate (CRA)\n- **Experience Level:** Junior - Senior","https://iqvia.wd1.myworkdayjobs.com/iqvia/job/Brussels-Brussels-Capital-Region-Belgium/Clinical-Research-Associate---Multi-Sponsor--Belgium_R1484456",{"id":67,"name":68,"urlSafeSlug":68,"logo":69},[821],{"city":822,"region":822,"country":823},"Brussels","Belgium","Candidates should possess a university degree in a scientific discipline or healthcare field, and experience in the pharmaceutical industry or clinical trials environment. Strong computer skills, including MS Office, are required, along with excellent command of Dutch, French, and English languages. The ability to establish and maintain effective working relationships, combined with organizational, time management, and problem-solving skills, is also necessary.","The Clinical Research Associate will perform site monitoring visits, conduct training to sites, manage subject recruitment plans, evaluate site practices, track regulatory submissions and approvals, and ensure proper documentation is maintained in the TMF and ISF. They will also collaborate with study team members, support the start-up phase of studies, and potentially manage site financial aspects according to clinical trial agreements. Additionally, the CRA will generate visit reports, submit follow-up letters, and resolve data queries, while adapting and driving recruitment plans in line with project needs.",{"employment":827,"compensation":829,"experience":830,"visaSponsorship":833,"location":834,"skills":835,"industries":842},{"type":828},{"id":111,"name":112,"description":18},{"minAnnualSalary":18,"maxAnnualSalary":18,"currency":18,"details":18},{"experienceLevels":831},[832],{"id":121,"name":122,"description":18},{"type":48},{"type":484},[836,837,838,673,726,839,731,840,841,730],"MS Office","Dutch","French","Subject Recruitment","TMF","ISF",[843,844],{"id":139,"name":200},{"id":139,"name":384},["Reactive",846],{"$ssite-config":847},{"env":848,"name":849,"url":850},"production","nuxt-app","https://jobo.world",["Set"],["ShallowReactive",853],{"company-IQVIA":-1,"company-jobs-c83c4a15-c7fa-4fd0-bbed-005308f4ab63-carousel":-1},"/company/IQVIA",{}]