Senior Clinical Research Associate
Minimum 2 years clinical monitoring experience (EU) or 3 years industry experience with 2 years monitoring and 1 year management (US). Bachelor's degree in life sciences preferred, strong knowledge of ICH GCP and regulations, ability to travel, CTMS/reputed company/eTMF experience, strong communication and leadership skills.
Key Responsibilities
- conducting monitoring
- reviewing reports
- mentoring CRAs
Skills & Tools
Clinical Trial Management System (CTMS), eTMF/TMF, electronic data capture
Job Details
- Category: Research and Development (R&D)
- Seniority: Senior Level
- Commitment: Part Time, Contract
- Workplace: Remote — France or Romania
- Languages: English
About reputed company
A global advisory firm providing consulting, research, and clinical development services to life sciences clients. — Industry: reputed company
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