Az álláshirdetés lejárt.
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  • A hirdetés 1340 napja lejárt


Location: Budapest (office-based)

Position Type: Full-time

As a Regulatory Submissions Coordinator with Medpace, you will have the opportunity to work with innovative therapeutic fields, with exposure to diverse clinical studies ranging from phase I – IV. This individual will be responsible for preparing, reviewing, and taking care of clinical trial applications and marketing applications to the international health agencies. In addition, this individual will ensure that submissions comply with applicable regulations and guidance documents. We are looking for proactive, positive and self-motivated individuals with a shared commitment to quality to join our supportive and dynamic team.   If you want to be a vibrant part of our growing team in Hungary please review this opportunity.



  • 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.



  • Bachelor's degree in life sciences;
  • Excellent organization and communication skills;
  • Knowledge of Microsoft® Office; and
  • Hands-on experience preparing, reviewing, and submitting regulatory documentation;
  • At least one year of work experience as a Regulatory Submissions Coordinator;
  • Fluency in English and Hungarian language

Travel: Minimal



Please access our career opportunities on our website at: Link megjelenítése, and apply for this position through our system. A member of our recruitment team will review your qualifications. If interested, you will be contacted for an interview.

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