Job Description

Mainz, Germany; London, United Kingdom; Munich, Germany | full time | Job ID: 9852





As aSenior Safety Scientist, you will provide scientific and strategic expertise to our clinical development programs at a compound level. Core responsibilities include safety data review, periodic report preparation, and oversight of the safety surveillance process.

Your main responsibilites are:

Provide expert scientific input to clinical safety activities, including safety database analyses, authoring and reviewing trial-related documents (e.g., Safety Management Plans, Reconciliation Plans, structured Benefit-Risk Assessments), and leading the preparation of periodic safety reports (e.g., DSURs) in collaboration with cross-functional teams. Partner with safety physicians to review and contribute to safety-relevant sections of clinical trial protocols, investigator brochures, clinical study reports, and statistical outputs (tables, figures, listings), and to co-author relevant safety documentation for BioNTech compounds. Drive the development, implementation, and continuous improvement of safety signal processes and oversee and enhance safety surveillance across clinical programs. Actively lead or contribute to BioNTech’s Safety Surveillance Teams (SST) and Safety Management Teams (SMT), including organizing and facilitating meetings to ensure consistent safety oversight and decision-making for assigned compounds. Serve as primary scientific point of contact for clinical safety team members assigned to clinical trials including best practice approaches, project-specific mentoring and training. Support collaboration by providing training and scientific guidance on safety management practices to colleagues in cross-functional departments. Build subject matter expertise in focus areas such as data analytics, signal detection, BRA, or literature review, and support regulatory interactions by contributing to authority requests and safety-related communications. Manage and update key standard operating procedures (SOPs) related to safety processes, ensure all safety management activities align with BioNTech’s quality standards, global regulations, and ethical requirements, and act as a Subject Matter Expert during audits and inspections for core safety processes.

What you have to offer:

Advanced Degree in life sciences, pharmacy, public health or a related field (PhD preferred) Minimum 5 years of experience in clinical research and pharmacovigilance within the pharmaceutical, biotech, or CRO industry, including case processing activities Strong knowledge of applicable regulatory, GCP, and GVP requirements in key geographies Experience in designing and implementing clinical safety processes, support systems, and tools Excellent scientific writing, project management, and cross-functional collaboration skills Strong computer proficiency, including experience in data visualization tools Fluent in written and spoken English

What we do with the BioNTainers:

We want to improve healthcare by making our innovations accessible worldwide. Therefore, we developed the first modular mRNA-manufacturing facilities based on a container solution called “BioNTainers”. Help us build a regional manufacturing network in Africa & Australia: With the region and for the region. As a part of the local team, driving the establishment of the regional end-to-end mRNA manufacturing solutions.

Benefits for you:

BioNTech is committed to the wellbeing of our team members and offers a variety of benefits in support of our diverse employee base. We offer competitive remuneration packages which is determined by the specific role, location of employment and also the selected candidate’s qualifications and experience.




Click here to find out more about what we do, the careers we offer ans also the benefits we provide. Note: The availability, eligibility and design of the listed benefits may vary depending on the location. The final requirements for the individual use of our benefits are based on the company's internal policies and applicable law.

How to apply:

Apply now by sending us your application documents including Curriculum Vitae, copy of ID, copies of degree certificates and professional certificates, motivation letter as well as your contact details via our online form.




Please note:


Only applications sent via our online form shall be considered. 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.




We are looking forward receiving your application.

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At BioNTech, we are more than just a biotechnology company – we are a community of innovators, scientists, and leaders dedicated to revolutionizing medicine by translating cutting-edge science into survival. Your contributions here have the potential to improve the health of people worldwide, especially by addressing diseases with high medical needs like cancer and various infectious diseases.


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Working at BioNTech means striving to achieve medical breakthroughs while growing your career in a meaningful way. Apply today and become part of a mission that has the potential to change lives around the world.


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