Director Clinical Development (all genders)

Cambridge, US; Berlin, Germany; Gaithersburg, US; London, United Kingdom; Mainz, Germany; New Jersey, US   |   full time   |   Job ID: 6951 

The Director Clinical Development will work hand-in-hand with the VP Clinical Development to implement clinical strategies and operationalize in both programs and clinical trials. You will work on the design and execution of clinical trials from early to late stage development through regulatory approval, horizontally leading a matrix team. This includes thorough data interpretation based on deep scientific and disease biology understanding, translational expertise and medical knowledge, including patient safety and data integrity.

Your main responsibilities are: 

• Works hand-in-hand with the VP of Clinical Development to guide clinical strategies and their operationalization into programs and trials.
• Drives the operational planning, content, execution and delivery for our programs and studies. Manages the day-to-day clinical activities for our clinical trials, including managing protocol amendments, overseeing data review activities, and communicating with investigators/sites as appropriate. 
• Assumes the responsibilities of Study Director when assigned as the clinical lead for a study; works hand-in-hand with the VP Clinical Development to develop and implement the CDP.
• As study lead, articulates TPP and CDP objectives to other development functions (e.g. Regulatory, Pharmacovigilance, Statistics, etc.) and drives alignment on objectives and expected outcomes. Drives translation of target product profile into clinical strategy.
• Collaborates with other development functions (e.g. Regulatory, Pharmacovigilance, Statistics, etc.) to support clarity on clinical objectives and drive alignment on objectives and expected outcomes.
• Responsible for medical/safety aspects of trials and risk/benefit assessments, supported by Clinical Trial Scientists and Pharmacovigilance. Works closely with Pharmacovigilance in the development of risk management plans.

What you have to offer: 

• M.D. with strong scientific and clinical background in Immuno-Oncology, Oncology and/or Infectious diseases.
• Several years of relevant experience in immuno-oncology, oncology and/or infectious diseases in a biotech/pharmaceutical and/or academic environment, including leadership of clinical development activities, ideally from exploratory Phase I/II clinical trials through late stage development in Phase III and NDA submission.
• Good understanding of clinical and scientific methods and approaches used in clinical development, from FIH to registration; experience with regulatory processes and registration a plus.
• Hands-on experience in managing the day-to-day clinical operations for the successful conduct of clinical trials.
• Experience in liaising with clinical operations and epidemiology on a regular basis for the efficient conduct of clinical trials.
• Experience in preparing and conducting interactions with global health authorities (e.g. EMA, FDA). Participation in drug development activities leading to successful registration is an advantage.
• Strong experience in monitoring and interpreting safety and efficacy clinical trial data and ensuring appropriate liaison for trial medical and patient safety issues.
• Functional and/or disciplinary leadership experience with a proven track record of leading teams is a plus.

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 Recruiter.

We are looking forward receiving your application.