Regulatory Submissions (Study Start Up) Coordinator

Medpace • madrid, comunidad de madrid, Spain • Posted May 21, 2026

Location madrid, comunidad de madrid
Job Type Full-time
Category Gestión y operaciones
Posted May 21, 2026

Our clinical operations activities are growing rapidly, and we are currently seeking a Regulatory Submissions Coordinator to join our Clinical Operations team in Spain. This position plays a key role in the clinical trial management process at Medpace. Please note that this is an office‑based position in Madrid . If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you.

Responsibilities

  • Prepare, review, and file initial clinical trial applications to regulatory authorities;
  • Prepare and submit responses to queries and amendments to clinical trial applications;
  • Ensure submissions comply with applicable regulations and guidance documents;
  • Advise team members on changing regulations and compliance requirements;
  • Maintain the Clinical Trial Management System and ensure timely filing of documents;
  • Collection ...

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