Clinical Research Physician - GU Oncology

Lilly • Indianapolis, IN

1d • $198,000 - $389,400

About The Position

The Clinical Research Physician (CRP), Clinical Development, provides scientific and clinical expertise to drive evidence generation and clinical strategy across Phase 1–3 programs. This role leads trial design and execution in close partnership with regulatory, statistics, NPP, medical affairs, and translational teams to deliver patient-focused outcomes.

Requirements

• Medical Doctor or Doctor of Osteopathy.
• Must be board eligible or certified in relevant field or have completed the comparable level of post-medical school clinical training relevant to the country of hiring.
• US trained physicians must have achieved board eligibility or certification.
• Physicians trained outside the US who are not US board eligible or certified may be hired directly for employment in the US at the discretion of the Chief Medical Officer.
• Non-US trained physicians must have completed education and training at a medical school that meets the requirements of the Liaison Committee on Medical Education (LCME). For the recognized list of foreign medical schools and the disapproved list, see PLA: Medical Licensing Information and Medical Education | MBC

Nice To Haves

• 3 years clinical and/or pharmaceutical industry experience
• Clinical development experience
• Experience supporting Phase I–III clinical programs
• Oncology in particular GU oncology experience
• Strong understanding of medical governance and regulatory requirements
• Demonstrated ability to communicate complex scientific data to diverse audiences
• Proven cross-functional collaboration and stakeholder engagement skills

Responsibilities

• Lead design and authoring of Phase 1–3 protocols with cross-functional input
• Ensure alignment of trial design (1°/2° endpoints, SOA, imaging, population, line of therapy, biomarker incorporation) with program goals across functional partners (regulatory, stats, NPP, medical affairs, CMC, translational)
• Support scientific advisory boards and steering committee meetings
• Design and execute enrollment plans including country and site selection, PI identification, and risk mitigation/trend monitoring
• Partner with Medical Affairs and NPP to support TPP and indication deliverables
• Proactively engage MSL teams for key insights and deliverables
• Primary author for clinical content development for regulatory submissions and meetings
• Author (with MW) disclosures
• Define and monitor success metrics; ensure cross-functional alignment
• Synthesize external data to inform trial design and strategy
• Primary owner/author in data presentation at internal governance meetings; support external presentations

Benefits

• company bonus (depending, in part, on company and individual performance)
• company-sponsored 401(k)
• pension
• vacation benefits
• eligibility for medical, dental, vision and prescription drug benefits
• flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts)
• life insurance and death benefits
• certain time off and leave of absence benefits
• well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities)

What This Job Offers

• Job Type: Full-time
• Career Level: Senior
• Education Level: Ph.D. or professional degree