Remote Medical Director, Oncology

Summary

Join Precision for Medicine as a Medical Director - Oncology to serve as the project physician and provide medical and scientific expertise to project teams, ensuring accuracy and integrity of data, with a focus on patient safety.

Requirements

• MD, DO, MBBS, or equivalent medical qualifications
• 5+ years of clinical experience
• 5+ years of experience in oncology clinical research
• Demonstrated expertise around the lifecycle of oncology drug development with ability to strategically analyze hematology clinical trial protocols
• Availability for domestic and international travel including overnight stays (approximate 30% travel requirement)

Responsibilities

• Work closely with senior leaders in Medical, Operational Strategy, and Business Development to support client engagement
• Support Business Development and Proposals teams by participating in the RFP process; prepare medical considerations section for proposals; and support or participate in bid defense meetings
• Write or edit scientific content of deliverables within budget and timelines
• Collaborates with Regulatory Affairs on regulatory product landscape and strategies as a part of overall drug development strategy
• Provide scientific insight and create content for specified company releases (e.g., white papers and publication manuscripts)
• Review and revise protocols, case report forms, training materials, project specific tools, analysis plans, study designs, clinical trial reports and new drug applications
• Review laboratory values, adverse events, coded adverse event and medication data, and data tables, listings and figures as needed
• Serve as a medical resource for study sites, the project team and clients
• Assist in the preparation of the Medical Monitoring Plan and materials for investigator meetings and staff training sessions
• Assume responsibility for medical and safety monitoring on assigned projects
• Participate in feasibility discussions relating to specific project proposals
• Develop training modules and provide training concentrating on disease states
• Participate in process improvement activities
• Collaborate with Senior Vice President, Global Medical and other members of the Medical Science Department to support growth and development activities globally

Preferred Qualifications

• Drug development experience in Hematology
• Oncology and/or Hematology Fellowship or equivalent
• Board Certification in Oncology and/or Hematology or equivalent
• Phase I and Phase II oncology clinical trial experience
• Prior CRO experience
• Maintains current scientific and medical knowledge base