Related skills
gcp edc ich etmf ctms📋 Description
- Serve as day-to-day operational contact for CROs and vendors.
- Track study deliverables and timelines; flag risks to leadership.
- Review CRO study documents for completeness and quality.
- Coordinate startup activities and regulatory document collection.
- Maintain trackers, timelines, and cross-functional visibility.
- Attend study team meetings; document minutes and follow-ups.
🎯 Requirements
- Bachelor’s degree; scientific/health-related field preferred.
- 6+ years in clinical operations or related field.
- Understanding of GCP, ICH guidelines, trial processes.
- Experience with CROs or clinical vendors in coordination.
- Strong attention to detail; manage multiple trackers and timelines.
- Familiarity with CTMS, EDC, and eTMF platforms.
🎁 Benefits
- Collaborative, fast-paced clinical operations team.
- Opportunities for sponsor-side career growth.
- Equity compensation and annual bonus eligibility.
- Competitive benefits package.
- Travel up to 20% for study needs.
- Remote-friendly work environment.
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