Clinical Research Physician – Oncologist

Overview

In this role you will provide medical leadership for oncology/solid tumor clinical trials, shaping study design and interpretation of results. You will act as Medpace’s medical expert across trial planning, regulatory documents, and manuscripts, ensuring rigorous safety and scientific standards. You will contribute to new clinical projects and collaborate with cross-functional teams to advance therapeutic development. This position offers hybrid work flexibility and a chance to drive impactful clinical research in a dynamic environment.

Pay / Benefits

• Flexible work environment
• Competitive compensation and benefits package
• Competitive PTO packages
• Structured career paths with opportunities for professional growth
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives

Responsibilities

• Provide medical management and expertise for clinical trials
• Contribute medical input to study reports, regulatory documents, and manuscripts
• Oversee safety and evaluation of trials in collaboration with team members
• Participate in new business development through proposals and sponsor meetings
• Coordinate with other departments through all study phases (feasibility, design, medical information, document review)
• Lead adherence to research-related protocols and policies

Key requirements

• MD in Medicine (required)
• Board certification and current medical licensure preferred
• Prior clinical trial research experience preferred
• Previous experience in pharmaceutical-related clinical research preferred

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