Our clinical operations activities are growing rapidly, and we are currently seeking a full-time office-based Regulatory Submissions Coordinator to join our Clinical Operations team in Munich. This position plays a key role in the clinical trial management process at Medpace. Entry-level positions with permanent contract are available for recent graduates.
Communicate with research sites in Germany, Austria and Switzerland (hospitals, etc.) Provide insightful input on regulatory submissions documents and maintain timelines for study start-up through both internal and external collaboration;
Advise on changing country regulations and compliance requirements; Bachelor's degree (preferably in a Life Sciences field);
Full professional proficiency in German and English in written and verbal communication;
Knowledge of Microsoft Office; We kindly ask to submit applications in English. We would appreciate if you could indicate the status of your work permit if needed.
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. Flexible work environment
Competitive compensation and benefits package
Structured career paths with opportunities for professional growth
Company-sponsored employee appreciation events
Employee health and wellness initiatives