Related skills
ms office gcp powerpoint edc ms project📋 Description
- Manage and deliver clinical elements across trials in multiple countries
- Lead CRAs and oversee trial quality, timelines, and scope
- Ensure regulatory documentation and sponsor communication
- Mentor and train team members
- Identify risks and propose action plans
- Maintain cross-functional partnerships to meet study priorities
- Lead CRAs in site relationships for high-quality oversight
🎯 Requirements
- Bachelor's degree or equivalent in science/health, oncology
- Experience leading multi-country clinical trials in CRO/Pharma/biotech
- Working knowledge of GCP/ICH guidelines and clinical development
- Availability for domestic and international travel
- Fluent English communication
- MS Office, MS Project, PowerPoint; CTMS, eTMF, EDC, IXRS
- Significant oncology trial management experience
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