We’re seeking a Regulatory Affairs Assistant to support our team in preparing, organizing, and submitting regulatory documentation. This is a remote, flexible role suited for a detail-oriented freelancer with regulatory affairs experience—particularly in pharmaceuticals, medical devices, or life sciences.
Responsibilities:
Support the preparation and submission of regulatory documents (FDA, ISO, CE Mark, etc.).
Maintain accurate records of regulatory filings and approvals.
Conduct regulatory research and monitor relevant global updates.
Help coordinate compliance communications between internal teams and external agencies.
Organize electronic documentation in accordance with QA and RA protocols.
Requirements:
Bachelor’s degree in life sciences or a related field.
At least 1 year of regulatory affairs or documentation experience.
Strong attention to detail, writing, and organizational skills.
Experience with remote collaboration tools (e.g., Slack, Google Drive, Zoom).
Knowledge of U.S. or EU regulatory standards preferred.
Submit your resume, hourly rate, and a brief message describing your experience.
This is a long-term engagement.