Clinical Research Coordinator
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Clinical Research Coordinator in Poitiers Working Hours: Part-time, 24h per week Start Date: Immediately Duration: Approximately 6 month IQVIA is currently recruiting a dedicated Clinical Research Coordinator to support a clinical research site in Poitiers. This part‑time position offers a unique opportunity to contribute to meaningful research in a collaborative and dynamic environment.
Key Responsibilities
- Maintaining and updating study documentation, including protocols, case report forms (CRFs), and Electronic Data Capture (EDC) systems
- Supporting patient screening and enrollment, including handling informed consent and privacy documentation
- Coordinating logistical activities for study procedures in line with the study protocol
- Performing data entry, quality checks, and resolving queries to ensure data accuracy and completeness
- Patient education
- Communicating with study monitors and responding to study‑related inquiries
- Carrying out general administrative tasks related to the study
Your Profile
- Bachelor’s degree in life sciences or equivalent education and/or relevant experience in a clinical or medical setting (e.g., clinical research coordinator, research assistant, nurse, medical assistant)
- Solid understanding of clinical trials and familiarity with study protocols, consent forms, and schedules
- good knowledge of medical terminology
- Strong IT skills, including proficiency in MS Office applications (Outlook, Word, Excel, Access)
- Must have at least 1-2 years experience working as a Clinical Research Assistant, Research Nurse or Clinical Research Coordinator at a clinical trial site
- Excellent interpersonal and communication skills
- Strong organizational skills and attention to detail
- Fluency in French and good command of English