Clinical Trials Feasibility Specialist

3 weeks ago


Cincinnati, Ohio, United States Medpace Full time

We are seeking a skilled Clinical Trials Feasibility Specialist to join our global clinical operations team.

This individual will provide strategic insights on country selection and enrollment planning for global clinical trials by working cross-functionally with our clinical operations, medical, and regulatory submissions teams.

Key responsibilities include coordinating feasibility assessments, delivering high-quality feasibility data, and supporting departmental process improvement initiatives.

Requirements include a Bachelor's degree in life sciences and the ability to prioritize multiple projects and tasks within tight timelines.

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.

We offer a hybrid work-from-home option, flexible work schedule, employee health and wellness initiatives, and structured career paths with opportunities for professional growth.

Our company is continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility.



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