Manager* CTSM IMPM
Open for hire at one of the following locations – Mainz Goldgrube, Cambridge Erie Street, London. - Job ID: 6099
Become a member of the BioNTech Family!
As a part of our team of more than 5.000 pioneers, you will play a key role in developing solutions for some of the most crucial scientific challenges of our age. Within less than a year, we were able to develop our COVID-19 mRNA vaccine following the highest scientific and ethical standards – writing medical history.
We aim to reduce the suffering of people with life-changing therapies by harnessing the potential of the immune system to develop novel therapies against cancer and infectious diseases. While doing so, we are guided by our three company values: united, innovative, passionate. Get in touch with us if you are looking to be a part of creating hope for a healthy future in many people's lives.
Manager* CTSM IMPM
Your main responsibilities are:
- Collaborate with external/internal stakeholders to improve clinical trial operations.
- Coordinate with CMC on product characteristics (volume/concentration)
- Collaborate with GCP Compliance to conduct CRO training.
- Translate clinical forecasts into kit needs/patient units and clinical needs
- Collaborates with CTSM functions (logistics, GxP, IRT) to determine trial design
- Share relevant trial-specific information with internal functions (e.g., planning, GMP operations, VM, IRT systems, logistics)
- Responsiblity for the execution of assigned clinical programs/studies
- Define trial design based on input from CTSM functions.
- Ensure that the trial design is followed across functions
- Provide trial specific input to process experts to support preparation of trial specific documents (e.g. Pharmacy Manual)
What you have to offer:
- Completed university education in supply chain management, pharmacy, chemistry, biotechnology, biochemistry, or a related discipline
- Relevant professional experience in clinical trial supply management or project management in the pharmaceutical or biotechnology industry, ideally in the areas of ClinDev, ClinOps or Clinical Supply
- Proven experience and track record in clinical trial management
- Knowledge of GCP principles (e.g., ethical principles, appropriate drug information, etc.)
- Knowledge of GMP principles (SOPs, documentation, etc.)
- Knowledge of IRT systems and standard office software (e.g. MS Office).
- Project management skills
- Very good English language skills
- Ability to solve multi-layered and dynamic tasks
- Self-motivation with strong problem solving and learning skills
- Ability to work accurately under pressure in a diverse environment
- Willingness and ability to take on responsibility and personal responsibility
Benefits for you
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.
Click here to find out more about what we do, the careers we offer and also the benefits we provide.
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.
Have we kindled your pioneering spirit?
This vacancy is to be hired at one of the following locations – Mainz Goldgrube, Cambridge Erie Street, London. Apply now for your preferred job and location through our careers site.
*BioNTech does not tolerate discrimination, favoritism, or harassment based on gender, political opinion, religion or belief, nationality, ethnic or social origin, age, sexual orientation, marital status, disability, physical appearance, health status or any other aspect of personal status. We are committed to creating a diverse and inclusive environment and are proud to be an equal opportunity employer. Most important – it’s a match!