CRA Virtual Info Session Event - Netherlands / Belgium

Medpace is hosting an Entry and Experienced CRA Networking Event where you can meet with Medpace CRA Managers to learn about Clinical Research Associate (CRA) openings near you.The Clinical Research Associate (CRA) at Medpace offers the unique opportunity to have an exciting career in the research of drug and medical device development while making a difference in the lives of those around them. For those with medical and/or health/life science interest and background who want to explore the research field and be part of a team bringing pharmaceutical and medical devices to market - this could be the right opportunity for you!

Please note you must be living in one of the participating countries, have local language and English fluency and have full right to work to be considered for this event.

WHEN : Thursday, November 7th at 4pm CET

WHERE: Virtual, Microsoft Teams

COUNTRIES:

• Netherlands (Rotterdam)
• Belgium (Leuven)

WHY MEDPACE?

• Competitive compensation, benefits program and bonus opportunities
• Annual merit increases
• In-House travel agents
• In-Country Managers and Mentors
• WFH flexibility (after 6 months)
• Extensive training and development available

**More details regarding the format of this virtual event will be provided should you be selected to attend.

• Conduct qualification, initiation, monitoring, and closeout visits for research sites in compliance with the approved protocol;
• Communication with the medical site staff including coordinators, clinical research physicians and their site staff;
• Verifying adequate investigator qualifications, training and resources, including facilities, laboratories, equipment, and staff;
• Medical record and research source documentation verification against case report form data, including informing the site staff of any entry errors, ensuring good documentation practices are being adhered to and communicating  protocol deviations appropriately per SOPs, GCP and applicable regulatory requirements;
• Verification that the investigator is enrolling only eligible subjects;
• Regulatory document review;
• Medical device and/or investigational product/drug accountability and inventory;
• Verification and review of adverse events, serious adverse events, concomitant medications and corresponding illnesses to confirm accurate data reporting in accordance with the protocol;
• Assessing the clinical research site’s patient recruitment and retention success and offering suggestions for improvement;
• Completion of monitoring reports and follow-up letters, which includes providing summaries of the significant findings, deviations, deficiencies,  and recommended actions to secure compliance.

PACE – MEDPACE CRA TRAINING PROGRAM

No research experience is needed as Medpace provides comprehensive initial and ongoing training, unmatched by other CROs.  Through our PACE Training Program, you will join other P rofessionals A chieving C RA E xcellence:

• PACE provides the platform to effectively and confidently carry out your duties, enhance your current abilities and ultimately help you become a high-functioning independent Medpace CRA.
• PACE will prepare you by developing your CRA skills through interactive discussions and hands on job-related exercises and practicums.
• To supplement your in-house and field-based training you may also participate in other clinical research departmental core rotations, learning other aspects of the drug/device development and approval process.

• Minimum of Bachelor's degree in life science related field; advanced degree preferred
• Previous experience as a clinical research coordinator is welcome.
• Willing to travel approximately 20-30% nationally
• Fluency in local language and excellent English
• Steady job tenure
• Full right to work in the country of residence
• Already residing permanently in the Netherlands or Belgium

We kindly ask to send applications in English.

Medpace is a full-service clinical contract research organization (CRO). We provide 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 its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.

When you join Medpace, you become part of a team dedicated to supporting the development of ground-breaking drugs and devices. Our employees provide hope for those living with debilitating diseases. We invite you to be a part of something that is impacting millions of people around the globe while enjoying a competitive total compensation and benefits package and internal growth opportunities.

Awards:

• Recognized by Forbes as one of America's Most Successful Midsize Companies in 2021, 2022, 2023 and 2024
• Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility

What to Expect Next:

A member of our recruitment team will review your qualifications and, if interested, you will be contacted for an RSVP.