Medical Director

Summary

Join Precision for Medicine as a Medical Director and work remotely from the UK, Spain, Poland, Hungary, Romania, Serbia, or Slovakia. You will serve as the project physician, providing medical and scientific expertise to project teams, ensuring data accuracy and patient safety. Responsibilities include collaborating with senior leaders, supporting business development, writing scientific content, collaborating with regulatory affairs, and serving as a medical resource. This role also involves reviewing documents, monitoring safety, developing training modules, and participating in process improvement. The position requires an MD, DO, MBBS, or equivalent, 5+ years of clinical experience, and 5+ years in oncology clinical research. Preferred qualifications include an oncology fellowship, board certification, and CRO experience.

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

Benefits

Remote work