Study Coordinator Clinical Research

vor 2 Wochen


München, Deutschland Medpace Vollzeit

Medpace Overview 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. As a Regulatory Submissions Coordinator you will have the opportunity to work within Regulatory Submissions, supporting our many projects and gaining some vital experience. You will be a productive member of the team office-based in Munich , and will be mentored and supported as you develop your skills. Working directly with Regulatory Submissions Coordinators, you will gain valuable hands-on experience to enable you to develop a career in clinical research.

Advise team members on changing regulations and compliance requirements;
A minimum of a Bachelor's degree is required (preferably in a Life Sciences field);
Knowledge of Microsoft Office;
Fluency in German and English;
We kindly ask to submit applications in English.



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