Entry-Level Clinical Research Associate Job at Medpace | Apply Now
A unique opportunity has arisen for aspiring Medpace Clinical Research Associate candidates in Munich, Germany. This role is ideal for candidates with a Life Science degree and clinical research experience who are eager to travel across Germany, Austria, and Switzerland while contributing to the development of pharmaceuticals and medical devices.
- Position: Clinical Research Associate
- Location: Munich, Germany
- Reference Number: 12351
About Medpace
Medpace is a full-service clinical contract research organization (CRO) providing phase I-IV clinical development services to the biotechnology, pharmaceutical, and medical device industries. Headquartered in Cincinnati, Ohio, Medpace employs more than 6,500 people across 40+ countries, focusing on accelerating the global development of safe and effective medical therapeutics through clinical research.
Medpace Clinical Research Associate Job Description
The Clinical Research Associate role at Medpace offers a chance to engage in drug and medical device development. This Medpace Clinical Research Associate position includes comprehensive training through the PACE Training Program, which equips professionals with the necessary skills to excel in their roles. This program emphasizes hands-on training and interactive discussions to enhance the abilities of Clinical Research Associates.
Eligibility Criteria
- Must have at least a B.Sc degree in Life Sciences.
- Must bring Clinical Study Coordinator / Clinical Study Nurse experience.
- Ability to travel 60-80%.
- Proficient knowledge of Microsoft® Office and general computer literacy.
- Detail-oriented and efficient in time management.
- Excellent verbal and written communication skills in German and English.
Key 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 adequate investigator qualifications, training, and resources.
- Ensure good documentation practices and communicate protocol deviations.
- Perform on-site and remote monitoring activities to identify site deviations.
- Verify that the investigator is enrolling only eligible subjects.
- Review regulatory documents and ensure accurate data reporting.
- Complete monitoring reports and follow-up letters summarizing findings and recommendations.
Why Medpace?
Medpace offers a collaborative culture where employees work alongside physicians, scientists, and industry-leading experts. The organization emphasizes continuous growth and development, providing defined career paths and ongoing training opportunities. Additionally, Medpace offers competitive compensation programs and comprehensive health, wellness, retirement, and PTO benefits.
The Medpace Clinical Research Associate role presents an exceptional opportunity for qualified candidates to advance their careers in clinical research. Interested individuals should apply at the earliest to be considered for this promising role.
