Related skills
ms office gcp powerpoint edc ms project📋 Description
- Manage clinical elements within a trial across multiple countries.
- Lead CRAs and oversee monitoring, regulatory, and data activities.
- Ensure timely delivery of trial deliverables and milestones.
- Communicate with cross-functional teams and sponsors to ensure quality.
- Mentor and train team members to grow capabilities.
- Identify risks and implement actions to protect study timelines.
- Build site relationships for high-quality oversight and data integrity.
- Oversee start-up, enrolment, and close-out processes.
🎯 Requirements
- Bachelor’s degree or equivalent in science/health; oncology exp.
- Lead clinical studies across multiple countries in CRO/Pharma as clinical lead.
- Significant oncology trial management experience.
- Working knowledge of GCP/ICH guidelines and clinical development.
- Travel availability for domestic and international trips.
- Fluent English communication.
- CTMS, eTMF, EDC, IXRS; MS Office, MS Project, PowerPoint.
- Strong cross-functional collaboration and relationship-building.
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