CRA Job Opportunity at Medpace | Apply Now
CRA job opportunities are growing rapidly in the global clinical research industry, and the latest opening at Medpace offers an excellent chance for fresh graduates and healthcare professionals to begin their journey in clinical trials. This exciting entry-level job in London allows candidates to gain hands-on experience in pharmaceutical and medical device research while receiving industry-leading training through the PACE® CRA Training Program. If you are searching for Medpace careers in clinical research, this opportunity could be the perfect start.
- Job Position: Entry-Level Clinical Research Associate (CRA)
- Company Name: Medpace
- Location: London
- Job ID: 11844
About the Company
CRA job seekers looking for global clinical research opportunities can explore excellent growth prospects at Medpace. Medpace is a full-service Clinical Research Organization (CRO) that provides Phase I-IV clinical development services to biotechnology, pharmaceutical, and medical device industries worldwide.
Headquartered in Cincinnati, Medpace employs more than 6,000 professionals across 40+ countries. The company focuses on accelerating the development of safe and effective medical therapeutics through scientific expertise and disciplined research approaches. Medpace specializes in several therapeutic areas including oncology, cardiology, endocrinology, metabolic disease, central nervous system disorders, anti-viral, and anti-infective research. Professionals interested in Medpace careers benefit from working in an innovative environment that supports learning, career progression, and global exposure in clinical research.
CRA Job Description
CRA job opportunities at Medpace are designed for candidates interested in pharmaceutical research, medical devices, and clinical trial monitoring. This entry-level job offers extensive hands-on training through the company’s renowned PACE® Training Program.
The Clinical Research Associate role involves monitoring clinical trial sites, ensuring protocol compliance, verifying patient safety, reviewing regulatory documents, and supporting research teams throughout the study process. Candidates will initially work fully office-based in the central London office to maximize training benefits before progressing further in the role.
PACE® CRA Training Program
CRA job training at Medpace is conducted through the specialized PACE® – Professionals Achieving CRA Excellence Program. The program helps candidates:
- Develop strong Clinical Research Associate skills
- Gain practical exposure through interactive discussions
- Participate in hands-on job-related exercises
- Build confidence in clinical monitoring activities
- Become independent and highly efficient CRAs
This training program makes this entry-level job highly attractive for freshers and healthcare professionals entering the clinical research industry.
Qualifications Required
CRA job applicants should possess educational qualifications and communication skills suitable for clinical research environments. Required qualifications include:
- Bachelor’s degree in Life Sciences or related field preferred
- Willingness to travel approximately 60–80% across the UK
- Familiarity with Microsoft Office tools
- Strong communication and presentation skills
- Valid driver’s license
- Willingness to remain fully office-based during the core training program
This entry-level job is especially suitable for fresh graduates looking to establish long-term careers in clinical research and pharmaceutical development.
Key Responsibilities – CRA Job
CRA job responsibilities at Medpace include managing and monitoring clinical trial activities while ensuring regulatory compliance and patient safety. Key responsibilities include:
- Conduct qualification, initiation, monitoring, and closeout visits for research sites
- Communicate with clinical research physicians, coordinators, and medical site staff
- Verify investigator qualifications, facilities, laboratories, equipment, and staffing resources
- Review medical records and research source documentation
- Ensure Good Clinical Practice (GCP) compliance and protocol adherence
- Identify and communicate protocol deviations appropriately
- Verify enrollment of eligible study participants only
- Perform regulatory document review and verification
- Maintain investigational product and medical device accountability
- Review adverse events and serious adverse events documentation
- Assess patient recruitment and retention strategies at research sites
- Prepare monitoring reports and follow-up letters with recommendations for compliance improvements
Why Choose Medpace Careers?
CRA job opportunities at Medpace provide professionals with exceptional learning experiences and long-term career growth in the CRO industry. Benefits include:
- Dynamic and fast-paced working environment
- Exposure to multiple therapeutic areas
- Collaboration with therapeutic and regulatory experts
- Structured promotion and career advancement opportunities
- Mentorship and management growth pathways
- Competitive salary and bonus programs
- Opportunities to travel and work across research sites
Professionals pursuing Medpace careers can contribute to research that improves patient lives globally while building expertise in clinical trials and drug development.
