Medical Monitor

Responsibilities

• Perform ongoing medical monitoring activities, including thorough medical data review.
• Draft protocols, related documents, and clinical development plans for new compounds to support regulatory approval.
• Manage day-to-day clinical activities, including protocol amendments and communication with investigators and sites.
• Oversee data review activities and ensure high medical quality and patient safety throughout clinical trials.
• Review Clinical Study Report (CSR) medical content to ensure it meets high medical standards.
• Collaborate with Clinical Operations and other cross-functional teams to balance trial complexity, time, and cost.

Requirements

• Doctor or master’s degree in medicine, pharmacy, or biology.
• Strong scientific and clinical background in Immuno-Oncology or Oncology.
• Minimum of 3 years of experience in biotech, pharmaceutical, or academic settings.
• Proven experience in medical monitoring, including overseeing and interpreting safety and efficacy clinical trial data.
• High proficiency in English (both written and spoken).
• Ability to work effectively in a global, cross-functional matrix environment.

About the Company

BioNTech is a biotechnology company dedicated to revolutionizing medicine by translating cutting-edge science into survival. We focus on addressing high medical needs, such as cancer and infectious diseases, through innovation and a passion for advancing medicine.