Clinical Research Coordinator - Poitiers
IQVIA · Poitiers, France
Clinical OperationsPart-timeCompany career page
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Role summary
IQVIA seeks a part-time Clinical Research Coordinator for a 6-month contract in Poitiers. The role involves managing study documentation, supporting patient enrollment, performing data entry, and coordinating trial logistics. Candidates need 1–2 years of clinical trial experience, fluency in French and English, and proficiency with medical terminology and standard office software.
What they're looking for
- Bachelor's degree in life sciences or equivalent clinical/medical experience
- 1-2 years experience as Clinical Research Assistant, Research Nurse, or Clinical Research Coordinator
- Knowledge of clinical trials, protocols, consent forms, and study schedules
- Proficiency in MS Office applications and medical terminology
- Fluency in French and good English command
- Strong organizational skills, attention to detail, and interpersonal abilities
What you'll be doing
- Maintain and update study documentation including protocols, case report forms, and EDC systems
- Support patient screening, enrollment, informed consent, and privacy documentation
- Coordinate logistical activities for study procedures per study protocol
- Perform data entry, quality checks, and resolve data queries for accuracy
- Provide patient education and communicate with study monitors regarding inquiries
Privacy & handoff
This role links to IQVIA's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.