The Clinical Research Associate position at Medpace presents a unique opportunity to build a rewarding career in drug and medical device development while positively impacting lives. This role is perfect for those with a medical or health/life science background who wish to explore research and contribute to bringing pharmaceuticals and medical devices to market.

About the Company

Medpace is a full-service clinical contract research organization (CRO) that provides phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through clinical research advancement. With over 6,500 employees across 40+ countries, we leverage regulatory and therapeutic expertise across major therapeutic areas including oncology, cardiology, metabolic, endocrinology, and more.

The Role

As a Clinical Research Associate, you will travel and engage in exciting work that enhances pharmaceuticals and medical devices. You will be part of a mid-sized CRO where you are not just a number, with a dynamic working environment and varying responsibilities. The role offers expansive experience across multiple therapeutic areas and the opportunity to work alongside a team of medical and regulatory experts.

Responsibilities

• Conduct qualification, initiation, monitoring, and closeout visits for research sites in compliance with the approved protocol.
• Communicate with medical site staff, including coordinators and clinical research physicians.
• Verify investigator qualifications, training, and resources.
• Ensure accurate medical record and research documentation against case report form data.
• Confirm eligibility of enrolled subjects and review regulatory documents.
• Manage medical device and investigational product accountability.
• Assess patient recruitment and retention success, providing suggestions for improvement.
• Complete monitoring reports and follow-up letters with significant findings and recommended actions.
• Collaborate effectively with Medpace's internal cross-functional teams.

Requirements

• Minimum Bachelor of Science in a Health or Life Science related field.
• At least 1 year of clinical research experience with direct patient-facing responsibility as a Clinical Research Coordinator, Clinical Study Coordinator, or similar role.
• Willingness to travel approximately 60-70% nationally.
• Familiarity with Microsoft® Office.
• Fluent in Dutch and English.
• Strong communication and presentation skills.
• Valid driver’s license.

What We Offer

• Competitive compensation programs that recognize and reward performance.
• Comprehensive health, wellness, retirement, and PTO benefits.
• Office-based culture with occasional work from home flexibility after training.
• Company-sponsored social events.
• Defined career paths with clear advancement opportunities and ongoing training.

What to Expect Next A Medpace team member will review your application, and if your profile matches our current needs, you will be contacted for an interview. While we review all applications carefully, we are unable to respond to every applicant, and only candidates selected for interviews will be contacted.