Related skills
gcp edc ip tmf ich-gcp📋 Description
- Oversees study site management to protect patient safety and data quality.
- Guides audit readiness and supports required follow-up actions.
- Updates and maintains trial management tools and status reports.
- Manages site start-up including feasibility, recruitment, and IRB submissions.
- Performs on-site and remote monitoring per protocol and SOPs.
- Documents activities, supports recruitment, and tracks action items.
🎯 Requirements
- Europe: life science/pharmacy degree or licensed health professional.
- America: 4-year degree in scientific/healthcare discipline.
- 2+ years as CRA in CRO/pharma or equivalent; site management
- Excellent communication and organizational skills; team player.
- Experience monitoring oncology trials.
- Travel up to 60% and international travel as needed.
🎁 Benefits
- Discretionary annual bonus
- Health insurance
- Retirement savings benefits
- Life and disability insurance
- Parental leave and paid time off
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