Related skills
ms office gcp edc ms project etmf📋 Description
- Manage clinical elements within a trial, incl. site start-up and enrolment.
- Oversee monitoring planning, data cleaning, and trial close-out.
- Lead CRAs to ensure high-quality site oversight and payments.
- Identify timeline risks and propose action plans with sponsors.
- Mentor and train team members for growth.
- Maintain cross-functional collaboration and timely communications.
🎯 Requirements
- Bachelor’s degree or equivalent in science/health, oncology preferred.
- Leading clinical trials across multiple countries in CRO/Pharma.
- Significant oncology trial management experience.
- Working knowledge of GCP/ICH guidelines and the clinical development.
- Willingness to travel domestically and internationally.
- Must communicate effectively in English.
🎁 Benefits
- Remote work options across Europe.
- Collaborative, fast-paced oncology-focused environment.
- Global cross-functional teams and growth opportunities.
- Exposure to precision medicine and data analytics.
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