Clinical Trials Assistant 1 at IQVIA

Buenos Aires, Buenos Aires, Argentina

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Not SpecifiedCompensation

Entry Level & New Grad, Junior (1 to 2 years)Experience Level

Full TimeJob Type

UnknownVisa

Clinical Research, PharmaceuticalsIndustries

Requirements

Bachelor Degree in Life Science or Healthcare
3 years administrative support experience or an Intern experience in clinical research or pharma
Written and verbal communication skills including good command of English language
Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint
Effective time management and organizational skills
Ability to establish and maintain effective working relationships with coworkers, managers, and clients
Awareness of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines as provided in company training
Knowledge of applicable protocol requirements as provided in company training

Responsibilities

Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) team with accurately updating and maintaining clinical documents and systems (e.g., Trial Master File (TMF)) that track site compliance and performance within project timelines
Assist the clinical team with the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures
Assist with periodic review of study files for completeness
Assist CRAs and RSU with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information
Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow
Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation
May accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training

Skills

Key technologies and capabilities for this role

Trial Master File (TMF)Clinical DocumentationMicrosoft WordMicrosoft ExcelMicrosoft PowerPointGood Clinical Practice (GCP)ICH GuidelinesAdministrative SupportTime ManagementRegulatory Compliance

Questions & Answers

Common questions about this position

What qualifications are required for the Clinical Trials Assistant role?

A Bachelor Degree in Life Science or Healthcare is required, along with 3 years of administrative support experience or intern experience in clinical research or pharma. Additional requirements include strong written and verbal communication skills in English, computer skills in Microsoft Word, Excel, and PowerPoint, effective time management, organizational skills, and awareness of GCP and ICH guidelines.

What are the main responsibilities of this position?

The role involves assisting CRAs and RSU teams with updating and maintaining clinical documents and Trial Master Files, preparing and handling clinical documentation, tracking Case Report Forms and data flow, acting as a central contact for project communications, and potentially accompanying CRAs on site visits after training.

Is the position full-time or part-time?

The position is full-time.

What is the salary or compensation for this role?

This information is not specified in the job description.

What experience makes a strong candidate for this role?

Candidates with a Bachelor’s degree in Life Science or Healthcare, 3 years of administrative support or intern experience in clinical research/pharma, and familiarity with GCP/ICH guidelines will stand out. Strong organizational skills, proficiency in Microsoft Office, and the ability to build effective working relationships are also key.

IQVIA

Advanced analytics and clinical research services

About IQVIA

IQVIA provides advanced analytics, technology solutions, and clinical research services specifically for the life sciences industry. Their services utilize extensive data resources and technology to create connections within healthcare, allowing clients to gain insights that help speed up the development and marketing of new medical treatments. This process is facilitated by their IQVIA Connected Intelligence™ system, which offers quick and flexible insights. IQVIA stands out from competitors by focusing on patient privacy, employing various technologies to protect individual data. The company's goal is to enhance healthcare outcomes by supporting biotech, pharmaceutical, and medical device companies, as well as researchers and government agencies, in understanding diseases and advancing medical science.

Durham, North CarolinaHeadquarters

1998Year Founded

$3,526MTotal Funding

POST_IPO_EQUITYCompany Stage

Cybersecurity, Biotechnology, HealthcareIndustries

10,001+Employees

Risks

Rapid advancement of cancer vaccines may disrupt traditional clinical research models.

Proliferation of disparate technological solutions causes technology overload in clinical trials.

Generative AI technologies face challenges in adoption due to data privacy concerns.

Differentiation

IQVIA leverages advanced analytics and big data for life sciences solutions.

The company offers privacy-enhancing technologies to protect individual patient data.

IQVIA's AI Assistant provides rapid, actionable insights for healthcare and life sciences.

Upsides

Increased adoption of decentralized clinical trials enhances patient-centric study designs.

AI-driven drug discovery accelerates identification of potential drug candidates.

Expansion of telemedicine facilitates remote patient monitoring and data collection.

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