Feasibility Coordinator Job at Medpace | Apply in Cincinnati – Apply Now!
Are you passionate about clinical research and data-driven strategy? Join Medpace, a global leader in clinical trials, as an Experienced Clinical Trials Feasibility Coordinator in Cincinnati, Ohio. This role combines clinical expertise with analytical insights to guide strategic site and country selection for global trials. Ideal for professionals with a background in life sciences and 3โ5 years of CRO feasibility experience, this position offers the chance to make a global impact on healthcare.
About the Company:
Medpace is a scientifically driven clinical contract research organization (CRO) headquartered in Cincinnati, Ohio. With over 5,000 employees in 40+ countries, Medpace provides end-to-end clinical trial services across therapeutic areas like oncology, cardiology, CNS, and infectious diseases. For over 30 years, Medpace has helped bring innovative therapies to patients globally.
Job Details:
Job Opening: Experienced Clinical Trials Feasibility Coordinator
Location: Cincinnati, Ohio
Department: Feasibility & Proposals
Job Code: 11103
Job Summary
We are currently seeking an Experienced Feasibility Coordinator to work collaboratively with our global clinical operations team. The ideal candidate will harness their clinical background, expertise in clinical research, and data analysis skills to provide strategic insights on country selection and enrollment planning for global clinical trials.
Responsibilities
- Coordinate feasibility assessments and provide high-quality feasibility data
- Develop proposal strategies for site and country selection
- Present feasibility results to the proposal team
- Coordinate outreach to investigative sites for feedback
- Assist with mentoring junior feasibility coordinators
- Collaborate with operational team for bid defense meetings
- Support process improvement initiatives and departmental functions
Qualifications for the Feasibility Coordinator Job
- Bachelor’s degree in life sciences required; Master’s or PhD preferred
- 3-5 years of feasibility experience in a CRO setting
- Analytical thinker with great attention to detail
- Ability to manage multiple projects under tight timelines
- Excellent written and verbal communication skills
Why Medpace?
At Medpace, we are driven by our dedication to improving patient lives and making a positive impact on healthcare. Join us to be part of a team that values people, purpose, and passion.
Cincinnati Perks
- Flexible work environment
- Competitive PTO packages
- Competitive compensation and benefits
- Employee appreciation events
- Health and wellness initiatives
- Community involvement
- Discounts on local attractions
- Structured career paths
- Discounted tuition for UC online programs
Keywords: Clinical Trials Feasibility Coordinator, Medpace, Cincinnati, Global Clinical Trials, Feasibility Research, CRO
