What are the responsibilities and job description for the Regulatory Content Manager for Pharmaceuticals position at GForce Life Sciences?
GForce Life Sciences is a leading provider of document management services to the pharmaceutical industry. We are seeking an experienced Regulatory Content Manager to join our team in Princeton, NJ.
Job Summary
We are looking for a highly skilled Regulatory Content Manager to assist with U.S policy and SOP lifecycle document development and management. The successful candidate will have experience with document management and/or project coordination with digital properties such as websites, intranets, and microsites.
About the Role
The ideal candidate will have 3 years of professional experience in a Pharma or other regulated environment. They will be responsible for tracking documents during the review/approval process, direct engagement with authors and teams, and following up with authors/teams to ensure deadlines are met.
Main Responsibilities
- Manage documents in the Inkling content management system (CMS).
- Editorial updates and review (e.g., ensuring updates align with document guidelines and other policies and SOPs).
- Assist with digital content management, including building new and updating existing policies and SOPs, fixing broken links, and QC revised documents to ensure updates align 1:1 with author updates submitted via Word.
- Assist with document authoring for new and updated policies.
- Assist with managing document development activities and deadlines.
- Manage document approvals/extensions via Veeva Vault.
Requirements
- Experience with document management and/or project coordination with digital properties such as websites, intranets, and microsites.
- 3 years of professional experience in a Pharma or other regulated environment.
Benefits
- Full time, 40 hours/week.
- Benefits available (Medical, Dental, Vision, 401k).
- Pay Range - $74k - $80k (Based on experience).
Salary : $74,000 - $80,000
