Medical Director - Oncology

MD, DO, MBBS, or equivalent medical qualifications 5+ years of clinical experience Completed an accredited medical residency program 5+ years of experience in oncology clinical research Demonstrated expertise around the lifecycle of oncology drug development Ability to strategically analyze oncology clinical trial protocols Availability for domestic and international travel (approx. 30%) Drug development experience in oncology (preferred) Oncology and/or Hematology Fellowship or equivalent (preferred) Board Certification in Oncology and/or Hematology or equivalent (preferred)

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 oncology development programs. Contribute to the development of the Medical team and support Business Development. Support client engagement and participate in RFP processes. Write or edit scientific content for deliverables. Collaborate with Regulatory Affairs on drug development strategies. Provide scientific insight for company releases. Review protocols, case report forms, training materials, and other study documents. Review laboratory values, adverse events, and data. Serve as a medical resource for study sites, project teams, and clients. Assist in preparation of Medical Monitoring Plan and investigator meeting materials. Assume responsibility for medical and safety monitoring on assigned projects. Participate in feasibility discussions. Develop training modules and provide training on disease states. Participate in process improvement activities. Support growth and development activities globally.