Associate Director, Clinical Science

Cambridge, US;
Gaithersburg, US;
London, United Kingdom;
New Jersey, US
full time
Job

As Associate Director, Clinical Science, you will be at the forefront of designing and executing oncology clinical trials that contribute to advancing BioNTech’s mission of developing innovative treatments. Your expertise will shape study designs and operational strategies, ensuring data integrity and compliance. Collaborating with cross‑functional teams in a dynamic environment, you will drive impactful clinical trial processes while fostering excellence within the clinical science team.

In this role, you will play a pivotal part in protocol development, trial execution, and engaging with scientific experts to inform clinical strategies. Your contributions will directly influence BioNTech’s goals and support robust medical governance across our programs.

• Lead protocol development and optimize clinical trial designs to assess investigational oncology drugs effectively.
• Collaborate with cross‑functional teams to develop comprehensive clinical development plans aligned with program strategies.
• Drive execution of global clinical studies while ensuring adherence to protocols, regulatory standards, and ethical guidelines.
• Engage with internal and external scientific experts to interpret emerging data and incorporate best practices into trial conduct.
• Monitor study progress, review data trends, resolve adverse events, and ensure compliance throughout the study lifecycle.
• Mentor junior colleagues to cultivate a culture of continuous improvement within the clinical science team.

• Bachelor’s degree in life sciences or healthcare; advanced degree preferred with 8+ years of clinical experience is required;
  Master’s, Pharm
  
  D, MPharm, PhD, MBBS, BDS, MD strongly preferred.
• Proven experience in clinical development within oncology or immuno‑oncology settings.
• Strong understanding of Good Clinical Practice (GCP) and all phases of drug development (Phase 1–3).
• Proficiency in planning and executing global clinical trials within pharmaceutical companies or CROs.
• Collaborative mindset with proven ability to work effectively in matrix environments and influence stakeholders without direct authority.
• Skilled in analyzing clinical data using tools like EDC platforms or Excel; experience in process optimization is desirable.

US based candidates expected Pay Range: $146,300/year to $234,100/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.

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.

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.

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 ‘Hire Right’. You will be informed accordingly by your BioNTech‑Recruiter.

We are looking forward receiving your application.