Related skills
ms office powerpoint edc ms project etmf📋 Description
- Manage site selection, start-up, enrollment, monitoring, data cleaning, close-out.
- Deliver successful trial execution and meet all deliverables.
- Coordinate regulatory docs and oversight with cross-functional teams.
- Mentor and train team members.
- Identify timeline risks and propose action plans.
- Lead CRAs to establish site relationships for monitoring and regulatory activities.
🎯 Requirements
- Bachelor’s degree in science/health or related field (oncology preferred).
- Experience leading multi-country clinical trials in CRO/Pharma/biotech (clinical lead).
- Extensive oncology trial management experience.
- Working knowledge of GCP/ICH guidelines.
- Willingness to travel domestically and internationally.
- English language proficiency.
🎁 Benefits
- Remote work option.
- Opportunity to work in precision medicine/oncology trials.
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