Related skills
gcp microsoft office edc ctms tmf📋 Description
- Support study sites and clinical teams per ICH-GCP and SOPs.
- Serve as site contact and perform core CRA duties across multiple studies.
- Assist in investigator recruitment, site feasibility, and questionnaire reviews.
- Manage site data in TMF and coordinate CTMS milestones.
- Ensure timely data entry in EDC and other required systems.
- May attend site visits and assist with Investigational Product accountability.
🎯 Requirements
- Bachelor's degree in science/healthcare (or international equivalent).
- Minimum 1 year relevant experience.
- Fluent in French and English (written and spoken).
- Proficient in Microsoft Office (Outlook, Word, Excel, PowerPoint).
- Working knowledge of the drug development process.
- Ability to travel as needed.
🎁 Benefits
- Remote-friendly work environment.
- Collaborative team culture.
- Mentorship of a junior CRA trainee.
- Opportunities to develop in clinical research.
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