Related skills
ms office gcp edc ms project etmf📋 Description
- Manage clinical trial elements: site start-up, enrolment, monitoring
- Ensure successful execution and deliverables
- Regulatory docs and oversight with cross-functional team
- Mentor and train team members
- Identify risks to study timelines; implement action plans
- Lead CRAs to establish site relationships for oversight
🎯 Requirements
- Bachelor’s degree in science/health; oncology preferred
- Experience leading multi-country clinical studies in CRO/Pharma/Biotech
- Significant oncology trial management experience
- GCP/ICH knowledge and clinical development process
- English proficiency; willingness to travel domestically/internationally
- CTMS/eTMF/EDC/IXRS; MS Office/Project
🎁 Benefits
- Remote work option
- Equal opportunity employer
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