U.S. Licensed Medical Director

Job Summary

U.S. Licensed Medical Director, this full-time position involves leading medical oversight for early-phase immune-oncology trials, ensuring patient safety and data integrity while managing clinical decision-making and safety reporting.

Key Responsibilities

• Provide real-time medical oversight and support to investigators regarding patient eligibility and clinical management
• Lead the identification and management of Immune-Related Adverse Events (irAEs) and develop safety management plans
• Conduct ongoing medical review of trial data and lead safety reporting, including the drafting of periodic safety reports

Required Qualifications

• M.D. or equivalent degree
• 3+ years of clinical research experience in a biotech/CRO or as a clinical investigator
• Proven expertise in managing patients treated with checkpoint inhibitors or T-cell engagers
• Proficiency with Electronic Data Capture (EDC) systems and experience in data cleaning and medical coding review
• Ability to manage multiple early-phase trials in a fast-paced environment