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).
Your Contribution:
* 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 Good Match:
* 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.
If the position is filled in the US, the Expected Pay Range is $113,600/year to $171,600/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. Compensation at other locations may vary significantly.
Your 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.
Note: The availability, eligibility and design of the listed benefits may vary depending on the location. The final requirements for the individual use of our benefits are based on the company's internal policies and applicable law.
How to apply:
Apply now by sending us your application documents including Curriculum Vitae, copy of ID, copies of degree certificates and professional certificates, motivation letter as well as your contact details via our online form.
Please note:
Only applications sent via our online form shall be considered. 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.
We are looking forward receiving your application.