Related skills
ms office gcp edc etmf ctms📋 Description
- Manage clinical elements across trials in multiple countries
- Lead CRAs and ensure study timelines and quality
- Oversee regulatory docs and cross-functional oversight
- Mentor and train team members
- Identify risks and propose mitigation plans
- Drive collaboration to achieve client satisfaction
🎯 Requirements
- Bachelor’s degree or equivalent in science/health fields
- Experience leading clinical aspects across multiple countries in CRO/Pharma/Biotech
- Significant oncology trial management experience
- Working knowledge of GCP/ICH guidelines
- Availability for domestic and international travel
- Fluency in English
🎁 Benefits
- Remote work options across Europe
- Mentoring and training of team members
- Autonomy and ownership to deliver outcomes
- Cross-functional collaboration for client satisfaction
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