Manager, Clinical Trial Supply Management IMPM
Cambridge, US; Gaithersburg, US; New Jersey, US | full time | Job ID: 10621
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).
Main Responsibilities:
- 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.
Qualifications:
- 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 ClinDev, ClinOps, 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.
Expected Pay Range (US): $113,600/year to $181,600/year + benefits, annual bonus & equity (bonus and equity is variable and dependent on company and individual performance). *Compensation for the role will depend on several factors, including responsibilities of the job, education, experience, knowledge, skills, and abilities.
Your Benefits:
BioNTech US is committed to employee wellbeing and offers best-in-class benefits & HR programs to support an inclusive & diverse workforce. Salaried/Position-Targeted Hourly Employees working 30+ hours per week are eligible for our comprehensive benefits package. Benefits include but are not limited to:
- 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
- Sitterstream: 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
…and more! More details to be shared.
Home to dozens of research institutions, biopharmaceutical companies, life science incubators, venture capital firms, and over 30 million square feet of laboratory space, Cambridge, Massachusetts has earned a reputation as the #1 life science cluster in the world. As part of the Greater Boston area, the city is often referred to as the "biotech supercluster" due to its high concentration of life sciences firms. This unique ecosystem is the result of a model partnership between academia and industry, fostering collaboration and innovation and driving the development of new therapies, medical devices, and diagnostics. As Cambridge’s thriving life sciences industry continues to evolve, the city remains a beacon of knowledge, innovation, and collaboration, poised to shape the future of science and technology.
Apply now - We look forward to your application!
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 ‘HireRight’. You will be informed accordingly by your BioNTech-Recruiter.