Study Start-up Specialist

☞ Medpace

Vue: 130

Jour de mise à jour: 12-11-2025

Localisation: Leuven Flemish Brabant

Catégorie: Administratif / Commis / Assistant R & D

Industrie: Pharmaceutical Manufacturing Hospitals Health Care Health Human Services

Niveau: Associate

Type d’emploi: Full-time

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le contenu du travail

Job Summary

Our clinical activities are growing rapidly, and we are currently seeking a full-time Regulatory Submissions Coordinator (Study Start Up Specialist) to join our Clinical Operations team. This position will work on a team to accomplish tasks and projects that are instrumental to the company’s success. 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 clinical trial applications to domestic and international regulatory agencies;
  • Ensure submissions comply with applicable regulations and guidance documents;
  • Advise sponsors on changing regulations and compliance requirements; and
  • Track submissions and ensure timely filing of documents.

Qualifications

  • Master’s or PhD degree in life sciences;
  • Experience as a Regulatory Submissions Coordinator for EC/RA applications in Belgium;
  • Excellent organization and communication skills;
  • Knowledge of Microsoft® Office;
  • Hands-on experience preparing, reviewing, and submitting regulatory documentation; and
  • Dutch and/or French and very good knowledge of English.

We kindly ask to submit applications in English.

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Date limite: 27-12-2025

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