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Clinical Research Associate II (French speaking)
Ergomed
Europe
Clinical Research
Site Management
French
Lead Clinical Research Associate - Contract
ProTrials
Global
Clinical Monitoring
Regulatory Compliance
Project Management
Responsibilities:
- Monitor and own the progress of clinical studies at investigative sites.
- Ensure studies are conducted, recorded, and reported per protocol, SOPs, ICH-GCP, and regulations.
- Coordinate all necessary activities to set up and monitor a study.
Qualifications:
- Life science degree and/or equivalent experience.
- 1 year or more as a CRA in a CRO or pharmaceutical/biotech industry.
- Site management or equivalent experience in clinical research.
Travel:
- Availability for domestic travel including overnight stays, up to 50-60%.
- International travel may be required for some senior level positions.
Culture:
- You are calm and thoughtful when things don't go as planned.
- You are well-prepared and always staying two steps ahead.
- You find quick and creative ways to overcome difficulties.
Precision for Medicine
Precision for Medicine integrates clinical trial execution with deep scientific knowledge, laboratory expertise, and advanced data sciences to improve the speed, cost, and success rate of bringing life-changing therapies to patients. They have a strong focus on Oncology and Rare Disease, and are proud to share extremely high CRA retention rates compared to industry averages.