Manager, Clinical Trial Supply Management IMPM

Manager, Clinical Trial Supply Management IMPM

BioNTech SE is inviting applications for the Manager, Clinical Trial Supply Management IMPM position.

Location:

Cambridge, US;
Gaithersburg, US;
New Jersey, US | 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.

• 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.

Expected Pay Range (US): $113,600/year to $181,600/year + benefits, annual bonus & equity (bonus and equity are variable and dependent on company and individual performance).

• Medical, Dental and Vision Insurance
• Life, AD&D, Critical Illness Insurance
• Pre‑tax HSA & FSA, DCRA Spending Accounts
• Employee Assistance & Concierge Program (EAP) available 24/7
• Parental and Childbirth Leave & Family Planning Assistance
• Sitter stream:
  Virtual Tutoring & Childcare Membership
• Paid Time Off:
  Vacation, Sick, Bereavement, Holidays (including Floating) & Year‑End U.S. Shutdown.
• 401(k) Plan with Company Match
• Tuition Reimbursement & Student Loan Assistance Programs
• Wellbeing Incentive Platforms & Incentives
• Professional Development Programs
• Commuting Allowance and subsidized parking
• Discounted Home, Auto & Pet Insurance

Apply for our Cambridge, US;
Gaithersburg, US;
New Jersey, US location and simply send us your documents using our online form.

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.