From Clinical Research Coordinator to CRA: Virtual Event

Looking for the next step in your career? Medpace is hosting a virtual event specifically for Clinical Research Coordinators / Study Nurses who aspire to become Clinical Research Associates: Take this great opportunity to learn about Medpace, connect with our CRA Managers and invest in your career and personal growth.

The Clinical Research Associate (CRA) role 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 patients. For those with medical and/or life science background who want to explore the clinical research field and be part of a team bringing pharmaceutical and medical devices to market - this is the right opportunity for you!

Requirements:

Please note you must be currently working as a Clinical Research Coordinator, Clinical Research Nurse or equivalent, living in Germany the with full right to work to be considered. If your application has been selected to attend, further details will be emailed to you prior to the event.

When : 29 June 2026, 15:00 – 16:00 CEST

Where: Virtual, Microsoft Teams*

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

• Travelling to study sites (Germany-wide) to conduct qualification, initiation, monitoring, and closeout visits 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 CRA 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:

• The training 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.
• It 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.

• Must have a minimum of a Bachelor’s degree in a health or science related field;
• Experience as a Clinical Research Coordinator (1 year);
• Ability to travel 60-70% to locations in the DACH region is required; some visits may be conducted remotely;
• Proficient knowledge of Microsoft® Office;
• Strong communication and presentation skills; and
• Must be detail-oriented and efficient in time management
• Excellent verbal and written communication skills in German and 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 6,000 people across 40+ countries.

People. Purpose. Passion. Make a Difference Tomorrow. Join Us Today.

The work we’ve done over the past 30+ years has positively impacted the lives of countless patients and families who face hundreds of diseases across all key therapeutic areas. The work we do today will improve the lives of people living with illness and disease in the future.

Medpace Perks

• Flexible work environment
• Competitive compensation and benefits package
• Competitive PTO packages
• Structured career paths with opportunities for professional growth
• Company-sponsored employee appreciation events
• Employee health and wellness initiatives

Awards

Continually recognized with CRO Leadership Awards from Life Science Leader magazine based on expertise, quality, capabilities, reliability, and compatibility.

What to Expect Next

A Medpace team member will review your qualifications and, if interested, you will be contacted with details for next steps.