Medical Monitor

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

Requirements

• 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)
• High proficiency in English (written and spoken)

Benefits

• Competitive remuneration package
• Variety of benefits in support of our diverse employee base