Regulatory Submissions Coordinator – Site Activation

Medpace; Buenos Aires; On-site; ARS 900,000 - 1,300,000; Full time

Job summary

Medpace in Buenos Aires is seeking a Regulatory Submissions Coordinator to join our Regulatory Submissions team. You will work on multiple projects and gain experience in regulatory processes while being mentored and supported for career development.

You will collaborate with Coordinators to collect essential documents, prepare submissions, and ensure deadlines are met, all while maintaining high quality and regulatory compliance across studies.

Qualifications

• Bachelor's degree in Life Sciences required.
• 1–3 years of regulatory submissions experience.
• Excellent organizational and prioritization skills.
• Knowledge of Microsoft Office.
• Strong attention to detail and written/oral communication.
• Fluency in spoken and written English.

Responsibilities

• Provide day-to-day support, collecting vital documents for ethics submissions and preparing study documents.
• Support Regulatory Submission Managers and Start Up teams to ensure deadlines are met.
• Conduct quality control of documents.
• Provide guidance to internal and external team members to ensure regulatory compliance.
• Perform other tasks as needed.

Skills

Organizational skills

Prioritization

Attention to detail

Oral and written communication

English fluency

Education

Bachelor's degree in Life Sciences

Tools

Microsoft Office

Job description

Medpace in Buenos Aires is seeking a Regulatory Submissions Coordinator to join our Regulatory Submissions team. You will work on multiple projects and gain experience in regulatory processes while being mentored and supported for career development.

You will collaborate with Coordinators to collect essential documents, prepare submissions, and ensure deadlines are met, all while maintaining high quality and regulatory compliance across studies.