Feasibility Manager

About the Role

We are seeking a Feasibility Manager to join our global clinical operations team. This role involves cross-functional collaboration with clinical operations, medical, commercial operations, and regulatory submissions teams, as well as analyzing data from internal and public sources to provide strategic insights on country selection, site recommendation, and enrollment planning for global clinical trials.

Responsibilities

• Conduct feasibility assessments for strategic or high-priority clients to support proposal development for new business opportunities, and provide high-quality, accurate feasibility data to internal and external teams.
• Present feasibility results to the proposal team to ensure correct assumptions were applied and strategy aligns with our therapeutic and operational experience.
• Coordinate outreach to investigative sites as needed to obtain indication- and protocol-specific feedback in support of feasibility strategy.
• Provide management, mentoring, training, and guidance to junior team members, including entry-level feasibility coordinators.
• Collaborate with project teams to support preparation for proposal documents and bid defense meetings.
• Suggest and implement improvements to the feasibility process, templates, and systems to ensure timely and accurate production of feasibility data, analysis, and text.

Requirements

• Bachelor’s degree in life sciences (Master’s or PhD preferred).
• Minimum 3.5 GPA.
• 5+ years of feasibility experience within a CRO.
• Prior experience managing staff.
• Analytical thinker with strong attention to detail.
• Ability to prioritize multiple projects and tasks within tight timelines.
• Excellent written and verbal communication skills.

Benefits

• Competitive compensation programs that recognize and reward performance.
• Comprehensive health, wellness, retirement, and PTO benefits.
• Office-based culture with occasional work-from-home flexibility for eligible positions after training.
• Company-sponsored social events and intramural sports.
• Modern corporate campus with on-site dining, free parking, and 24/7 fitness and wellness facilities.

About the Company

Medpace is a full-service clinical contract research organization (CRO) providing Phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through clinical research excellence. We leverage in-country regulatory and therapeutic expertise across major areas, including oncology, cardiology, metabolic, endocrinology, central nervous system, and anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, Medpace employs over 6,500 people across 40+ countries.

Work Culture

• Purpose-Driven Work: Collaborate with physicians, scientists, and industry-leading experts to advance medical therapeutics through clinical research.
• Collaborative Culture: Contribute to an interactive team environment that encourages decision-making, creative thinking, and continuous learning.
• Leadership Accessibility: Leadership is approachable and fosters open communication and mutual trust.
• Growth & Development: Defined career paths, clear advancement opportunities, and industry-renowned onboarding and training programs. Ongoing learning opportunities throughout your career.