Manager CTSM IMPM

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Cambridge, US;
London, United Kingdom | full time | Job

Drive Clinical Supply Excellence Across Global Trials. Play a pivotal role in ensuring investigational medicines reach patients on time and in full compliance. Shape processes that accelerate innovative therapies worldwide. Manage and co-define initiatives of all Clinical Trial Supply Management IMPM activities in global Phase I-III clinical trials (R&D Programs).

• Lead the coordination and execution of assigned clinical programs/trials, acting as the primary interface between CTSM internal functions and trial teams.
• Serve as the point of contact for other departments (e.g., GCO, CMC, PM, GRA), attend cross-functional meetings, and ensure trial set‑up requirements are followed across functions.
• Own and maintain the Clinical Supply Summary, consolidate information from various departments, and ensure consistency and accuracy across trial‑related documents (e.g., CDP, CTP, IB, Monitoring Plan, IMPD/IND sections).
• Liaise with internal and external stakeholders to improve clinical trial processes, align with CMC on product properties, and translate clinical forecasts into kit demand/patient units.
• Prepare IMP and IRT sections for investigator meetings, liaise with GCP Compliance for CRO trainings, and ensure adherence to ethical and regulatory standards.
• Manage and coach Specialist CTSM IMPM team members, fostering a culture of collaboration, innovation, and accountability.

• A relevant university degree in Supply Chain Management, Pharmacy, Chemistry, Biotechnology, Biochemistry, or a related discipline.
• At least 3 years of experience in Clinical Trial Supply Management or Project Management within the pharmaceutical or biotech industry, ideally in Clin Dev, Clin Ops, or Clinical Supply.
• Proven track record in managing clinical trials, with knowledge of GCP and GMP principles.
• Proficiency in IRT systems and standard office software (e.g., MS Office). Strong project management skills and the ability to solve multi‑layered, dynamic challenges.
• Business‑professional English language proficiency.
• A strong work ethic, problem‑solving mindset, and openness to exploring new topics and setting trends.

Join a team that values agility, creativity, and accountability. Together, we deliver therapies that transform lives and set new standards in clinical trial supply management.

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.

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.

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

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 ‘Hire Right’. You will be informed accordingly by your BioNTech‑Recruiter.

We are looking forward receiving your application.

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…