Full-time

Experienced Study Start Up Specialist

Posted by Medpace • Mexico, Ciudad de México, Mexico

📍 Mexico, Ciudad de México 🕒 February 25, 2026

About the Role

Join Medpace at our Mexico City office! As a Regulatory Submissions Coordinator you will have the opportunity to work within Regulatory Submissions, supporting our many projects and gaining vital experience in study start up! You will be a productive member of the team, 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.

Responsibilities

  • Provide day-to-day departmental/project support activities, such as collection of vital documents for ethics submissions and preparation of study documents to competent authorities;
  • Support Regulatory Submission Managers and Start Up teams in ensuring deadlines are adhered to;
  • Conduct quality control of documents;
  • Provide advice and guidance to internal and external team members to ensure compliance with applicable regu...

Ready to Apply?

Submit your application today and take the next step in your career journey with Medpace.

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