Manager Medical Science Liaison Oncology
Munich, Germany | full time | Job ID:10560As a Manager Medical Science Liaison Oncology, your main role is to establish collaborations with external healthcare professionals/experts, scientific opinion leaders and institutions to share and discuss evidence-based medical and scientific information about our oncology portfolio. You act as the field subject matter expert in oncology, while planning and executing stakeholder engagement and informing trial sites as needed.
Your responsibilities:
- Act as a field medical expert, delivering continuous medical education to HCPs (Healthcare professionals) in Germany and gathering actionable insights to inform strategy.
- Build and maintain scientific partnerships with key opinion leaders, Cooperative Study Groups, medical associations, and research organizations in oncology.
- Develop and execute an Medical Science Liaison (MSL) Oncology strategy aligned with local and European medical affairs priorities.
- Build and expand relationships/networks with key medical and scientific experts in the field of breast cancer and/or lung cancer.
- Support clinical trials by identifying study sites, participating in SIVs (Site Inviations Visits), assisting with patient enrollment, and ensuring smooth information exchange.
- Identify research opportunities, including Investigator-Initiated Trials, Real-World Evidence, and other evidence-generation studies.
- Represent the organization at scientific conferences, advisory boards, and educational events, sharing insights and preparing reports for internal stakeholders.
- Ensure timely documentation of HCP interactions, compliance with local policies, and accurate reporting of insights and safety information.
What you have to offer:
- Advanced degree (PhD, MD, or Pharmacist) with at least 5 years of experience in Medical Science Liaison (MSL) or Medical Affairs roles in Germany.
- Minimum 3 years of experience and an established network in Breast Cancer and/or Lung Cancer therapeutic areas, ideally within a pharmaceutical company.
- Strong expertise in GCP-compliant clinical trial support, with a solid understanding of trial design and execution.
- Exceptional ability to process, communicate, and present complex medical and scientific information effectively.
- Proven self-management and project management skills to independently plan and execute stakeholder engagement.
- Highest ethical standards with knowledge of clinical regulations, industry standards, and German codes of conduct.
- Fluent in German and English, with an entrepreneurial mindset, passion for innovation, and a “can-do” attitude.
Your Benefits:
- Your flexibility: flexible hours | vacation account
- Your growth: Digital Learning | Performance & talent development | leadership development | Apprenticeships | LinkedIn Learning
- Your value: Your voice at the table | Culture on an equal footing | Opportunities to shape & impact | Support for your full potential
- Your health and lifestyle: Company bike
- Your mobility: Job ticket | Deutschlandticket
- Your life phases: Employer-funded pension | Childcare
Apply now - We look forward to your application!
Job ID 10560 (please always specify if you have any questions)
By submitting your application, you acknowledge that a background check will be conducted as part of the recruitment process in accordance with applicable laws and regulations. If you are considered for the position, BioNTech will conduct the background check through our service provider ‘HireRight’. You will be informed accordingly by your BioNTech-Recruiter.
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