Clinical Research Jobs at Medpace, USA
Are you exploring high-impact clinical research jobs that combine travel, innovation, and career growth? This Clinical Research Associate opportunity at Medpace in the USA is ideal for life science professionals and PhD candidates eager to contribute to cutting-edge drug and medical device development while building a long-term career in clinical research.
About Medpace
Medpace is a global, full-service Clinical Research Organization (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 across 40+ countries, supporting therapeutic areas including oncology, cardiology, CNS, endocrinology, infectious disease, and more.
Job Details:
- Job Title: Clinical Research Associate (PhD Candidates)
- Job ID: 11096
- Location: Cincinnati, Ohio
- Category: Clinical Research Associate
Clinical Research Job Summary
Medpace is seeking Clinical Research Associates (CRAs) to join its team in Cincinnati, Ohio. This role offers an exciting opportunity for PhD candidates and life science professionals to launch a career in clinical research while contributing to the development of pharmaceuticals and medical devices that improve patient lives.
Through Medpace’s industry-leading PACE® CRA Training Program, candidates will receive comprehensive training—no prior clinical research experience required.
Medpace CRA Training Program (PACE®)
PACE® (Professionals Achieving CRA Excellence) is Medpace’s structured, hands-on training program designed to prepare CRAs for independent success.
Program Highlights:
- Comprehensive in-house and field-based CRA training
- Interactive discussions, practicums, and job-related exercises
- Exposure to other clinical research functions through departmental rotations
- Ongoing therapeutic training by in-house physicians and regulatory experts
Key Responsibilities
- Conduct site qualification, initiation, monitoring, and closeout visits
- Communicate with investigators, coordinators, and site staff
- Verify investigator qualifications, site resources, and staff training
- Perform source data verification and ensure protocol compliance
- Monitor sites using risk-based and centralized monitoring approaches
- Review regulatory documents and investigational product accountability
- Verify adverse event and safety reporting
- Assess patient recruitment and retention strategies
- Prepare monitoring reports and follow-up documentation
Qualifications for Clinical Research Jobs
Required:
- Bachelor’s degree in a health or life sciences field
- Ability to travel 60–70% nationwide (less for remote monitoring)
- Valid driver’s license
- Proficiency with Microsoft Office
- Strong communication, presentation, and time-management skills
- High attention to detail
Preferred:
- PhD or advanced life sciences background
- Minimum 1 year of healthcare-related work experience
Compensation & Benefits for Clinical Research Jobs
- Competitive base pay
- Travel bonus
- Equity/stock option program
- Training completion and retention bonuses
- Annual merit increases
- 401(k) matching
- Flexible work hours and work-from-home options
Additional Perks
- Retain airline and hotel reward points
- Home office furniture allowance
- Laptop and mobile phone with hotspot
- In-house travel agents and TSA PreCheck reimbursement
- Leadership opportunities (Lead CRA, CRA Manager, CTM, Training Manager)
- Administrative support at all CRA levels
- Opportunities to work with international CRA teams
Cincinnati Campus Perks
- Flexible work environment
- Competitive PTO (20+ days starting)
- Comprehensive benefits package
- Employee appreciation events
- Wellness initiatives
- Community engagement opportunities
- Discounts on local sports, fitness, and attractions
- Modern eco-friendly campus with on-site fitness center
- Structured career development paths
- Discounted tuition for University of Cincinnati online programs
Why Become a CRA at Medpace
- Dynamic, fast-paced role with varied day-to-day responsibilities
- Exposure to multiple therapeutic areas
- Work alongside regulatory and therapeutic experts
- Defined career progression and promotion ladder
- Competitive compensation and industry-leading perks
