Associate Director, Clinical Trial Supply Management IMPM

BioNTech SE • Cambridge, MA

36d

About The Position

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). What we do with the BioNTainers: We want to improve healthcare by making our innovations accessible worldwide. Therefore, we developed the first modular mRNA-manufacturing facilities based on a container solution called "BioNTainers". Help us build a regional manufacturing network in Africa & Australia: With the region and for the region. As a part of the local team, driving the establishment of the regional end-to-end mRNA manufacturing solutions. BioNTech, the story 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 various infectious diseases. Experience a dynamic workplace that embraces diversity in all its forms. We foster innovation, encourage creativity, and develop business strategies driven by our shared passion for advancing medicine. Working at BioNTech means striving to achieve medical breakthroughs while growing your career in a meaningful way. Apply today and become part of a mission that has the potential to change lives around the world. BioNTech does not tolerate discrimination, favoritism or harassment based on gender, political views, religion or belief, nationality, ethnic or social origin, age, sexual orientation, marital status, disability, physical appearance, health status or any other physical or personal characteristics. 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! BioNTech - As unique as you

Requirements

• 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.
• 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.

Nice To Haves

• Background in Project Management and Operations is preferable.

Responsibilities

• 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.

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: Director
• Industry: Chemical Manufacturing
• Number of Employees: 1,001-5,000 employees