Manager Clinical Trial Supply Management IMPM

BioNTech • Cambridge, MA

5d

About The Position

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).

Requirements

• 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.

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.

Benefits

• 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.

What This Job Offers

• Job Type: Full-time
• Career Level: Manager