• Serve as the project physician and provide medical and scientific expertise to project teams • Ensure the accuracy and integrity of the data resulting from the trial, with concentrated focus on patient safety • Participate in the strategic planning and execution of critical development programs for a variety of clients in oncology or autoimmune disease • 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 • Collaborate 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