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. Ability to deliver on commitments and understand service culture. Strategic thinker. High degree of professionalism. Communicate effectively in English (verbally and written). Conduct formal presentations. Strong visual and presentation skills. Ability to work effectively in a fast-paced team setting with minimal supervision. Proven efficiency in working remotely.

Serve as project physician and provide medical/scientific expertise. Ensure accuracy and integrity of trial data and patient safety. Participate in strategic planning for development programs. Support client engagement and Business Development activities. Write/edit scientific content for deliverables. Collaborate with Regulatory Affairs on drug development strategy. Provide scientific insight for company releases. Review and revise protocols, case report forms, training materials, reports, and applications. Review laboratory values, adverse events, and data. Serve as a medical resource for sites, 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 on disease states. Participate in process improvement activities. Support global growth and development activities for the Medical Science Department.