Shanghai, China | full time | Job ID: 10161

The Medical Monitor will work together with Director Clinical Development for the assigned programs. He/ She will work on medical data review, draft protocol and related documents and execution of clinical trials from early to late-stage development through regulatory approval. 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:

• Responsible for ongoing medical monitoring activities including medical data review
• Drafts protocol and related documents and execution of clinical trials of their assigned programs, helping to create the clinical development plan for new compounds, and pave a path towards regulatory approval.
• Works together with the Director Clinical Development in programs and trials.
• Manages day-to-day clinical activities for our clinical studies including management of protocol amendments, overseeing data review activities and communicating with investigator / sites where appropriate.
• Ensures at the program and trial level, that the clinical development team works together with Clinical Operations team, with a focus on patient centric drug development, ensuring balancing of high medical quality, trial complexity, as well as time and cost considerations.
• Reviews Clinical Study Report (CSR) medical content and ensures it meets high quality expectations on medical standards, provides respective guidance to other members of the clinical development team
• Contributes to a collaborate culture within and outside Clinical Development and actively manages best practice sharing and capability building within the clinical team.

What you have to offer:

• Doctor or master’s degree major in medicine, pharmacy or biology with strong scientific and clinical background in Immuno-Oncology, Oncology
• Minimum of 3 years of experience within Immuno-Oncology, Oncology at the biotech/pharmaceutical and the academic setting,
• Strong medical experience in medical monitoring including overseeing and interpreting safety and efficacy clinical trial data.
• High level of comfort and demonstrated successes working in a matrix environment (global and cross-functional), including contributing to establishing clarity and structures and driving state of the art collaborations with external academic and industry partners.
• A genuine interest and understanding of the science supporting the clinical development programs. Confident to discuss and present scientific and mechanistic aspects of drug development.
• High proficiency in English (written and spoken)

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

We are looking forward receiving your application.