Clinical Research Coordinator - Poitiers
On-sitePoitiers, Nouvelle-Aquitaine, France
Poitiers, Nouvelle-Aquitaine, FranceOn-sitePart TimeBachelors DegreeEnterprise
Part TimeBachelors DegreeEnterprise
Job Summary
Maintain and update study documentation, including protocols, case report forms, and Electronic Data Capture systems. Support patient screening and enrollment by handling informed consent and privacy documentation while coordinating logistical activities for study procedures. Perform data entry, quality checks, and resolve queries to ensure accuracy, and communicate with study monitors regarding inquiries. Carry out general administrative tasks and provide patient education. This part-time role (24 hours/week) begins immediately for a six-month duration at an IQVIA site in Poitiers.
Required Qualifications
- Bachelor's degree in life sciences or equivalent education and/or relevant experience in a clinical or medical setting
- Solid understanding of clinical trials
- Familiarity with study protocols
- Familiarity with consent forms
- Familiarity with schedules
- Good knowledge of medical terminology
- Strong IT skills
- Proficiency in MS Office applications (Outlook, Word, Excel, Access)
- 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
- Attention to detail
- Fluency in French
- Good command of English
- Part-time, 24h per week
- Start Date: Immediately
- Duration: Approximately 6 month
- Truthful and complete information and credentials submitted in application
- Zero tolerance policy for candidate fraud
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