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Entry Clinical Trials Feasibility Specialist – Cincinnati, Ohio

0-2 years
Not Disclosed
10 Nov. 21, 2025
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Entry Clinical Trials Feasibility Specialist – Cincinnati, Ohio

Location: United States – Cincinnati, Ohio
Category: Feasibility & Proposals


About the Role

Medpace, a global full-service clinical contract research organization (CRO), is seeking an Entry Clinical Trials Feasibility Specialist to join our global clinical operations team. This role plays a key part in supporting country selection, site feasibility, and enrollment planning for international clinical trials. The specialist will work cross-functionally with clinical operations, medical, regulatory, and proposal teams to provide strategic insights based on internal and public data sources.

This position is ideal for early-career professionals with a life sciences background and a passion for clinical research, data analysis, and global trial planning.


Key Responsibilities

  • Conduct feasibility assessments and deliver accurate, high-quality data to internal and external stakeholders.

  • Develop preliminary proposal strategies for country and site selection in global clinical trials.

  • Present feasibility findings to proposal teams, ensuring assumptions align with therapeutic and operational experience.

  • Coordinate outreach to investigative sites for indication- or protocol-specific feedback when required.

  • Assist project teams in preparing for bid defense meetings.

  • Support departmental process improvement initiatives and general administrative functions.


Required Qualifications

  • Bachelor’s degree in Life Sciences (Master’s or PhD preferred).

  • Strong analytical skills with meticulous attention to detail.

  • Ability to prioritize multiple projects and deliver results under tight timelines.

  • Excellent written and verbal communication skills.

  • Passion for clinical research and early career interest in global trial operations.


Preferred Qualifications

  • Familiarity with clinical trial feasibility and site selection processes.

  • Understanding of global regulatory and operational requirements in clinical research.

  • Experience with data analysis and reporting for clinical study planning.


About Medpace

Medpace is a full-service CRO providing Phase I-IV clinical development services across biotechnology, pharmaceutical, and medical device industries. Headquartered in Cincinnati, Ohio, Medpace employs over 5,000 professionals in 40+ countries. Our mission is to accelerate the development of safe and effective therapeutics through a scientific and disciplined approach, leveraging deep expertise across therapeutic areas including oncology, cardiology, metabolic disease, CNS, anti-viral, and anti-infective research.


Why Medpace?

  • Impactful work improving the lives of patients worldwide.

  • Flexible work environment and modern, eco-friendly campus.

  • Competitive compensation and PTO packages, starting at 20+ days.

  • Health and wellness initiatives and employee appreciation events.

  • Career development opportunities with structured growth paths.

  • Community engagement and discounts for local attractions, gyms, and sports events.

  • Tuition discounts for UC online programs.


Awards and Recognition

  • Named a Top Workplace 2024 by The Cincinnati Enquirer.

  • Recognized by Forbes as one of America’s Most Successful Midsize Companies (2021–2024).

  • Recipient of multiple CRO Leadership Awards from Life Science Leader magazine.


Experience Required

  • Entry-level role, suitable for candidates with a Bachelor’s in Life Sciences and some relevant internship, research, or early professional experience.

  • Strong analytical and communication skills required.

  • Ability to work collaboratively in a fast-paced, global clinical research environment.


Next Steps

Qualified candidates will be reviewed by a Medpace team member, and selected applicants will be contacted with details on the next steps in the hiring process.


SEO & GPT Optimization Notes:

This version is optimized for keywords such as: Clinical Trials Feasibility, Entry-Level Clinical Research, Medpace Cincinnati, Global Clinical Operations, Site Selection, Feasibility Specialist, Clinical Trial Planning, CRO Jobs USA. It also emphasizes location (Cincinnati, Ohio), remote/global collaboration, and early career opportunities, which helps improve both geo-targeting and candidate reach on global job portals.