Entry-Level Clinical Trial Job at Medpace in the USA
An exciting opportunity is available for an Entry Clinical Trials Feasibility Specialist at Medpace Careers in Cincinnati, Ohio. This Entry-Level Clinical Trial Job in the USA is ideal for life science graduates interested in clinical research and global trial planning. The position involves working with global clinical operations teams to analyze data, support feasibility strategies, and provide insights that guide country and site selection for international clinical trials.
About the Company:
Medpace is a full-service Contract Research Organization (CRO) providing Phase I–IV clinical development services to biotechnology, pharmaceutical, and medical device companies. Headquartered in Cincinnati, the company employs more than 5,000 professionals across 40+ countries.
Medpace focuses on accelerating the global development of safe and effective therapeutics through a strong scientific and disciplined approach. The company has deep expertise across therapeutic areas, including oncology, cardiology, metabolic diseases, endocrinology, central nervous system disorders, antiviral therapies, and anti-infective research.
Job Details:
- Job Title: Entry Clinical Trials Feasibility Specialist
- Location: Cincinnati
- Department: Feasibility & Proposals
- Job ID: 11871
- Industry: Clinical Research / Life Sciences
- Experience Level: Entry Level
- Work Environment: Flexible work environment
Key Responsibilities:
- Coordinate feasibility assessments and deliver high-quality, accurate feasibility data to internal and external teams in this Clinical Trial Job in USA.
- Develop preliminary proposal strategies for site and country selection in global clinical trials.
- Present feasibility results to proposal teams to ensure correct assumptions and alignment with therapeutic and operational experience at Medpace Careers.
- Coordinate outreach to investigative sites to obtain indication- and protocol-specific feedback when required.
- Assist project teams with preparation for bid defense meetings.
- Support departmental process improvement initiatives.
- Perform general administrative functions to support departmental operations.
Educational Requirements for this Job:
- A bachelor’s degree in Life Sciences or a related field is required.
- A master’s degree or a PhD is preferred but not mandatory.
Skills Required:
- Strong analytical thinking and attention to detail.
- Ability to manage multiple projects and tasks under tight timelines.
- Excellent written and verbal communication skills.
- Ability to work collaboratively with cross-functional teams, including clinical operations, medical teams, and regulatory experts.
- Strong organizational and data analysis abilities.
Benefits of the Clinical Trial Job:
- Flexible work environment and modern workplace facilities.
- Competitive paid time off packages starting at 20+ days.
- Competitive salary and benefits package.
- Company-sponsored employee appreciation events.
- Employee health and wellness initiatives.
- Opportunities for community involvement with nonprofit organizations.
- Discounts on local sports games, gyms, and attractions.
- Modern eco-friendly campus with an on-site fitness center.
- Structured career paths and professional growth opportunities.
- Discounted tuition programs for university online courses.
- Opportunity to work at an award-winning CRO recognized by The Cincinnati Enquirer as a Top Workplace in 2024 and recognized by Forbes as one of America’s Most Successful Midsize Companies.
