CRA Job Opportunity at Medpace | Apply Now
CRA job opportunities are growing rapidly in the global clinical research industry, and this Entry-level Clinical Research Associate role at Medpace offers an exciting opportunity for life science professionals to build a rewarding career in clinical trials and drug development. This opportunity in Belgium is ideal for candidates interested in pharmaceutical research, medical devices, and patient-focused healthcare innovation. With comprehensive training, career growth opportunities, and exposure to international clinical research projects, Medpace careers continue to attract talented professionals worldwide.
- Job Position:Â Entry-level Clinical Research Associate
- Job Location: Leuven, Belgium
- Job ID: 12182
About the Company
CRA job opportunities at Medpace provide professionals with the chance to work in a globally recognized clinical research organization. Medpace is a full-service Clinical Research Organization (CRO) that delivers Phase I-IV clinical development services to biotechnology, pharmaceutical, and medical device industries.
The company focuses on accelerating the development of safe and effective medical therapeutics through scientific expertise and disciplined research practices. Medpace operates across multiple therapeutic areas including oncology, cardiology, endocrinology, metabolic disease, central nervous system disorders, anti-viral, and anti-infective research.
Headquartered in Cincinnati, Medpace employs more than 6,000 professionals across 40+ countries worldwide. Medpace careers are known for offering excellent training, career progression, and global exposure in the clinical research industry.
CRA Job Description
CRA job roles at Medpace are designed for candidates who are passionate about clinical research, pharmaceuticals, and medical device development. This position provides an opportunity to work directly with research sites and healthcare professionals while contributing to the development of innovative therapies and treatments. The role is suitable for candidates from various healthcare and science-related backgrounds, including:
- Nurses
- Dieticians
- Pharmacists
- Biomedical Researchers
- Pharmaceutical and Device Sales Representatives
- Biotech Engineers
- PhD/Pharm.D Candidates
- Research Coordinators
- Research Nurses
This life sciences job also includes participation in the Medpace PACE Training Program, which provides extensive hands-on training and mentorship for aspiring Clinical Research Associates.
PACE – Medpace CRA Training Program
CRA job training at Medpace is provided through the PACE (Professionals Achieving CRA Excellence) Training Program. No prior research experience is required because Medpace offers comprehensive onboarding and continuous professional development. The PACE program helps candidates:
- Develop CRA skills through interactive learning
- Gain practical clinical research experience
- Build confidence in site monitoring activities
- Enhance communication and regulatory knowledge
- Become independent Clinical Research Associates
Qualifications
CRA job candidates should possess strong scientific knowledge, communication skills, and a willingness to travel for clinical monitoring visits.
Required
- Minimum Bachelor of Science degree in Life Science-related field
- Excellent command of English, Dutch, and French
- Strong communication and problem-solving skills
- Willingness to travel approximately 60–70% nationally
- Valid driver’s license
- Familiarity with Microsoft Office
Key Responsibilities
CRA job responsibilities include managing and monitoring clinical trial activities while ensuring compliance with study protocols and regulatory guidelines. Responsibilities Include:
- Conduct qualification, initiation, monitoring, and closeout visits for research sites
- Communicate with clinical research coordinators, physicians, and site staff
- Verify investigator qualifications, training, facilities, and research resources
- Review medical records and source documentation against case report forms
- Ensure Good Clinical Practice (GCP) and SOP compliance
- Verify patient eligibility and enrollment accuracy
- Perform regulatory document review
- Manage investigational product and medical device accountability
- Review adverse events, serious adverse events, and concomitant medications
- Assess patient recruitment and retention performance
- Complete monitoring reports and follow-up documentation
- Collaborate with international cross-functional Medpace teams
Why This CRA Job Stands Out
CRA job roles in Belgium provide candidates with the opportunity to contribute to groundbreaking pharmaceutical and medical device research while developing long-term careers in clinical research. This job in Belgium is ideal for professionals seeking:
- International clinical research exposure
- Career advancement in CROs
- Extensive CRA training
- Opportunities in pharmaceutical development
- Long-term growth in the life sciences industry
