Regulatory Manager
Precision For MedicineUnited States
Posted February 17, 2026
106000 - 151000 USD
Full Time
About the Company
Precision Medicine Group is an Equal Opportunity Employer. Employment decisions are made without regard to race, color, age, religion, sex, sexual orientation, gender identity, national origin, disability, veteran status or other characteristics protected by law.
Job Description
The Regulatory Manager provides regulatory development advice and guidance for optimal conduct of clinical trials, ensuring timely preparation of well organized, quality regulatory submissions in compliance with applicable regulations. The RM coordinates and prepares regulatory documents for submission to Regulatory Authorities and/or Ethics Committees, as applicable.
Requirements
- Provides regulatory guidance throughout the clinical development life cycle
- Compile, coordinate and review applications to Regulatory Authorities
- Develops and/or reviews documents intended for submission to the Regulatory Authorities and/or Ethics Committees
- Serve as representative of Global Regulatory Affairs at project team meetings
- Oversee and coordinate Regulatory Affairs Specialists
- Maintenance of project plans, project trackers and regulatory intelligence tools
- Assist in development of Regulatory Affairs Specialists and other operational area staff
- Provide input, as required, into regulatory strategy and timeline development for new study opportunities
- Participates in maintaining and executing on the corporate quality initiatives across business units within clinical solutions
Benefits
- Discretionary annual bonus
- Health insurance
- Retirement savings benefits
- Life insurance
- Disability benefits
- Parental leave
- Paid time off for sick leave and vacation
