Associate Director Clinical Trials | Pharmacist (m/w/d)
BioNTech SE
Job Summary
This Associate Director role involves leading the operational and administrative execution of complex, large-scale national and international clinical trials, primarily within oncology. The successful candidate will manage program timelines, oversee Clinical Research Organizations (CROs) and vendors, and ensure rigorous adherence to local laws, international guidelines (ICH GCP), and SOPs. Daily activities include leading cross-functional project teams, managing communications, escalating issues, and maintaining inspection readiness throughout the clinical program lifecycle. This position requires a strong background in pharmaceutical/biotech clinical development, significant experience leading global teams, and expertise in using various electronic data systems (eTMF, EDC). It is an attractive opportunity for a seasoned professional to drive critical clinical development programs in a dynamic, international environment.
Required Skills
Education
Bachelor’s degree in the life sciences or a university degree in a related field. Advanced degree preferred. PMP or equivalent certification desirable.
Experience
- Minimum 10 years in pharmaceutical, biotech, or related industry
- At least 6 years experience in Global Clinical Development leading cross-functional teams
- Experience leading one or more complex/large scale clinical trial/s in either early or late stage clinical development
- Oncology experience required
- Registrational trial experience preferred
Languages
Additional
- Willingness to work in Mainz, Germany or London, United Kingdom. Background check required as part of the recruitment process.
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