Clinical Research Coordinator - Madrid at IQVIA

Madrid, Community of Madrid, Spain

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Not SpecifiedCompensation

Junior (1 to 2 years)Experience Level

Part TimeJob Type

UnknownVisa

Clinical Research, HealthcareIndustries

Requirements

BS/BA in life sciences or educational equivalent and/or relevant work experience in a clinical environment or medical setting, e.g. clinical research coordinator, nurse, medical assistant, other medical profession
Basic knowledge of clinical trials, combined with in-depth knowledge of departmental, protocol and study-specific operating procedures, consent forms, and study schedules
Basic knowledge of medical terminology
Strong IT competence, skilled in using MS Windows and Office applications such as Access, Outlook, Excel, and Word
Excellent interpersonal skills with the ability to establish and maintain effective working relationships with co-workers, managers and client
Good organizational skills with the ability to pay close attention to detail

Responsibilities

Support clinical research studies and maintain a safe study environment according to health and safety policies under the direction and delegation of the Principal Investigator
Safeguard the well-being of subjects, act as a volunteer advocate, and address subject’s concerns
Maintain up-to-date study protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems, and other study documents
Plan and coordinate logistical activity for study procedures according to the study protocol
Perform clinical set-up and preparation for the study including labeling specimen collection tubes and containers, inventory of required supplies, and setting up or troubleshooting equipment and/or study issues
Assist with data entry, data quality checking, and query resolution to ensure adherence to study protocol and quality control for content accuracy and completeness
Assist in study enrollment by recruiting, screening, and orienting volunteers according to the study protocol
Correct custody of study drug according to site standard operating procedures
Coordinate with study monitor on study issues and effectively respond to monitor-initiated questions

Skills

Key technologies and capabilities for this role

Microsoft ExcelMicrosoft WordMicrosoft OutlookMicrosoft AccessClinical TrialsMedical TerminologyElectronic Data CaptureCase Report FormsMS Office

Questions & Answers

Common questions about this position

Is this a full-time or part-time position?

This is a part-time position.

What is the salary for this Clinical Research Coordinator role?

This information is not specified in the job description.

What education and experience are required for this role?

A BS/BA in life sciences or educational equivalent is required, along with relevant work experience in a clinical environment or medical setting, such as clinical research coordinator, nurse, or medical assistant.

What key skills are needed for the Clinical Research Coordinator position?

Strong IT competence with MS Windows and Office applications (Access, Outlook, Excel, Word), excellent interpersonal skills for building relationships, and good organizational skills with attention to detail are required. Basic knowledge of clinical trials, medical terminology, and study procedures is also needed.

What does IQVIA do as a company?

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries, helping accelerate innovative medical treatments to improve patient outcomes.

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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