Offer summary
Qualifications:
Solid independent monitoring experience in France as a CRA focused on complex clinical trials, Experience in various therapeutic areas including oncology, Familiarity with applicable regulatory requirements and IT proficiency, Effective time management skills and ability to maintain strong relationships while possessing excellent communication abilities in French and English.
Key responsabilities:
- Overseeing site management and ensuring compliance with protocol procedures and regulations
- Reviewing, verifying, and protecting study data, initiating actions to achieve project goals
- Serving as the primary contact for trial vendors
- Handling the entire process of Serious Adverse Event reporting and efficiently resolving data issues