Associate Director CTSM IMPM

Associate Director, Clinical Trial Supply Management IMPM

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

Lead Global Clinical Supply Strategies that make a difference. Orchestrate portfolio-level supply strategies for global clinical trials, ensuring patients receive the therapies they need—on time and without compromise. Define and lead initiatives of all Clinical Trial Supply Management IMPM-Portfolio activities in global Phase I-III clinical trials (R&D Programs).

Your Contribution:

• Define and lead initiatives for CTSM portfolio activities, ensuring alignment with platform portfolio strategies and clinical trial requirements.
• Develop and oversee distribution, manufacturing, and supply planning strategies for platform portfolios.
• Manage performance objectives and performance management for trials within the platform portfolio.
• Ensure platform portfolio requirements are followed across all related clinical trials.
• Oversee planning activities at the platform portfolio level, orchestrating the needle-to-needle supply process.
• Liaise with interfaces to address trial escalations and prioritizations.
• Provide CTSM feasibility perspectives to platform portfolio core teams.
• Provide guidance to Managers IMPM during trial setup, execution, and closeout phases.
• Train new team members to follow SOPs and ensure adherence to IMPM standards.
• Ensure compliance with GCP and GMP principles, as well as Quality Management Systems.
• Coordinate and compile regulatory documents, ensuring accuracy and consistency.
• Build and maintain strong relationships with internal and external stakeholders, ensuring alignment and effective communication.

A good match:

• A relevant university degree in Pharmacy, Chemistry, Biotechnology, Biochemistry, or a related discipline. Doctorate preferred, if applicable.
• At least 5 years of experience in Clinical Trial Supply Management within the pharmaceutical or biotech industry.
• Proven track record in managing multiple trial platforms and portfolios, as well as developing platform portfolio strategies for clinical trials.
• Background in Project Management and Operations is preferable.
• Deep knowledge of GCP and GMP principles, including SOPs, documentation, and ethical standards.
• Proficiency in IRT systems and standard office software (e.g., MS Office).
• Extensive knowledge of performance management in IMPM and Quality Management Systems.
• Ability to lead individuals with diverse professional backgrounds and expertise levels.
• Strong decision-making skills, strategic thinking, and negotiation abilities.
• Business-professional English language proficiency.

How to apply:

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.

BioNTech is committed to creating a diverse and inclusive work environment. We are proud to be an equal opportunity employer. The main thing is that you suit us, and we suit you!