BioNTech SE develops immunotherapies to fight cancer and infectious diseases, improving global health.
Open Positions
Senior Director, Clinical Science - Oncology
Bachelor's degree in life sciences/healthcare/nursing req. 12+ yrs exp in clinical development, with proven track record. GCP knowledge is essential, plus strong leadership & data management skills
CTSM Manager
Relevant education in Logistics/Supply Chain Mgmt. 3+ yrs experience in relevant industry. Proven distributor/performance mgmt skills
Senior Manager, Global Development Quality Assurance
3+ years of experience in GCP, 1+ year of experience in business partner relations, advanced degree in Life Sciences
Associate Director Facility Management Cluster Mainz (m/w/d)
Requires 2+ years of experience. Technical education with specialty (engineer, admin, specialist etc.) and a long career. Strong administrative/business knowledge & fluency in English
Specialist Clinical Trial Insurance
University degree preferred, insurance experience a must, strong knowledge of insurance regulations. Fluent in English and German required
Associate Technician Facility Management
Technical vocational training, relevant professional experience, familiarity with ERP and CAFM systems
Director GMP Production (m/w/d)
Pharmaceutical or biotechnological background, 10+ years of experience, strong leadership skills
Director Statistical Programming (Oncology)
Bachelor's degree in Statistics, Mathematics, Computer Science or related discipline. 15+ years (10+ years for advanced degree) experience in a pharmaceutical industry, CRO or another clinical research setting, with a focus on oncology. Excellent knowledge of statistical programming in SAS
Director GMP Production
Completed studies in pharmacy, biotechnology or related field, and experience in leading GMP production processes, as well as knowledge of legal requirements
(Senior-) Director, Clinical Development
MD with strong background in Immuno-Oncology or Oncology. 5-10 years of clinical development experience in Europe or US, including trials to NDA submission. Strong medical experience with clinical trial data
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