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Job Summary

Join Medpace in our Buenos Aires office! As a Regulatory Submissions Coordinator you will have the opportunity to work within Regulatory Submissions, supporting our many projects and gaining some vital experience. 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 regulations and requirements;
- Perform other tasks as needed.

Qualifications





- Bachelor's degree is required (preferably in a Life Sciences field) and at least 1-3 years of regulatory submissions experience;
- Excellent organizational and prioritization skills;
- Knowledge of Microsoft Office;
- Great attention to detail and excellent oral and written communication skills; and
- Fluency in spoken and written English.

We kindly ask to submit applications in English.

Benefits

Perks (vary by location and position):

- On-site fitness center(s)
- Campus walking paths
- Company-sponsored social and wellness events
- Official Sponsor of FC Cincinnati
- Hybrid work-from-home options and versátil work schedule
- On-site Market Place
- Free and covered parking
- Discounts for local businesses
- On campus restaurantsand banks coming soon

EO/AA Employer M/F/Disability/Vets

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📌 Site Activation Coordinator (Buenos Aires)
🏢 Medpace
📍 Buenos Aires