Associate Director Clinical Trials

Associate Director Clinical Trials

Locations: Mainz, Germany; London, United Kingdom. Full‑time position. Job ID: 9864.

As Associate Director Clinical Trials you are responsible for the execution of clinical trials, mainly with regard to operational and administrative aspects. This implies the preparation and processing of national and international projects under consideration of the local laws, international guidelines (ICH GCP) and applicable SOPs. You perform activities related to heading a project team, the supervision/control of third‑party providers, the timely performance of all services, as well as problem management by interacting with all departments involved.

Your Main Responsibilities Are

• Lead one or more complex/large‑scale clinical trials in either early or late‑stage clinical development within a program.
• Lead communications, issue escalations and help the teams within the program to further develop.
• Manage the Clinical Research Organization (CRO) and vendor(s) as it relates to clinical program level deliverables.
• Manage clinical study timelines for the program(s).
• Ensure inspection readiness throughout the clinical program lifecycle.

What You Have To Offer

• A Bachelor’s degree in the life sciences or a university degree in a related field with experience in the health industry (Advanced degree preferred).
• Minimum 10 years of experience in the pharmaceutical/biotech or related industry with at least 6 years experience in Global Clinical Development leading cross‑functional teams.
• Oncology experience required, registrational trial experience preferred.
• Knowledge and experience working with legislation and international guidelines (ICH‑GCP/CFR) for the performance of clinical research projects.
• Good communication and presentation skills both written and spoken inclusive of confident, articulate, and professional speaking abilities.
• Able to communicate strategy and decisions across different functions.
• Standard use of Project Management skills including teamwork, analytical and problem‑solving, time management and organizational skills, risk and cost management, and performance monitoring.
• Skilled in using Microsoft Office programs (Word, Excel, PowerPoint, MS Project) as well as good working knowledge of electronic data systems and technical solutions such as eTMF, IWRS, EDC, etc. and developing presentation material.
• High level of problem solving skills and able to proactively recognize risks and develop mitigations.
• PMP or equivalent certification desirable.

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 are 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 your application documents including Curriculum Vitae, copy of ID, copies of degree certificates and professional certificates, a motivation letter, and 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 to receiving your application.