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ms office edc oncology etmf ctms📋 Description
- Manage clinical trial elements across sites and countries.
- Oversee site selection, start-up, enrolment, monitoring and data cleaning.
- Ensure regulatory docs, oversight, and close-out activities.
- Lead CRAs and maintain high-quality monitoring across studies.
- Mentor team members and mitigate timeline risks.
🎯 Requirements
- Bachelor's degree in science or health-related field.
- Experience leading multi-country trials in CRO/pharma.
- Working knowledge of GCP/ICH guidelines.
- Willingness to travel domestically and internationally.
- English language proficiency.
- Proficiency with MS Office, MS Project, CTMS, eTMF, EDC, IXRS.
🎁 Benefits
- Remote work option across multiple European countries.
- Opportunity to work on cutting-edge precision oncology trials.
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