Senior Medical Director, Oncology

Leading the execution of early and late-stage clinical trials for oncology products, the full-time Senior Medical Director, Oncology will design study protocols, oversee medical monitoring, and ensure compliance with regulatory requirements while working remotely. Key responsibilities: Support the establishment of clinical trial strategies and design study protocols in compliance with regulations Act as medical monitor for company-sponsored trials, assessing eligibility and safety events Collaborate with internal teams to analyze safety data and prepare reports for regulatory agencies Required qualifications: MD with a minimum of 8 years post-residency relevant experience in oncology or hematology/oncology Extensive drug development experience in the biotechnology or pharmaceutical industry Hands-on experience in the design and execution of controlled clinical trials in oncology Understanding of basic science relevant to clinical oncology, such as biochemistry and molecular biology Ability to develop and maintain relationships with key opinion leaders in the field