Medical Director/Senior Medical Director

MD, DO, MBBS, or equivalent medical qualifications. 5+ years of Oncology clinical experience. Ability to strategically analyze oncology clinical trial protocols. Availability for domestic and international travel (approx. 30%). Experience working as a Medical Director for a CRO or Pharmaceutical company (preferred). Oncology Fellowship or equivalent (preferred). Maintains current scientific and medical knowledge base (preferred). Proven efficiency in working remotely (skills/competencies).

Serve as the project physician and provide medical/scientific expertise. Ensure accuracy and integrity of trial data, focusing on patient safety. Participate in strategic planning and execution of development programs. Contribute to the development of the Medical team and support Business Development. Support client engagement and the RFP process. Write or edit scientific content for deliverables. Collaborate with Regulatory Affairs on drug development strategy. Provide scientific insight and create content for company releases. Review and revise clinical trial documents. Review laboratory values, adverse events, and data. Serve as a medical resource for study sites, project teams, and clients. Assist in preparing Medical Monitoring Plans and training materials. Assume responsibility for medical and safety monitoring. Participate in feasibility discussions. Develop training modules concentrating on disease states. Participate in process improvement activities. Support global growth and development activities.