Entry-Level Regulatory Submissions Coordinator
Core
Prepare, review, and file clinical trial applications for France; communicate with research sites to collect essential documents for patient enrollment; ensure submissions comply with regulations.
Role type
Entry-level Regulatory Submissions Coordinator
Builds
Clinical trial regulatory submissions for France
Domain
Clinical research / Biopharmaceuticals
Deliverable
client delivery
Required skills
Regulatory submission preparation, document collection from research sites, timeline management, compliance monitoring, knowledge of country regulations, Microsoft Office proficiency
Preferred skills
Life Sciences degree background, interest in drug development
Technologies
Microsoft Office
Responsibilities
Prepare, review, and file clinical trial applications for France; Communicate with research sites in France to collect essential documents; Provide input on regulatory submissions documents and maintain timelines; Ensure submissions comply with applicable regulations; Advise on changing country regulations; Track submissions and ensure timely filing.
Seniority
Entry-level, recent graduate
