Regulatory Manager/ Senior Regulatory Manager (Clinical Trials)
Precision for Medicine(1 month ago)
About this role
This role sits within the Regulatory Affairs function of a CRO focused on oncology and rare disease, providing expert regulatory input across the clinical development lifecycle. The position supports timely, compliant regulatory interactions and submissions, represents Global Regulatory Affairs to project teams and business development, and contributes to corporate quality initiatives. The role also involves mentoring regulatory specialists and maintaining regulatory intelligence to inform strategy.
Required Skills
- Regulatory Guidance
- Clinical Development
- Regulatory Submissions
- Document Review
- Regulatory Strategy
- Agency Meetings
- Orphan Designation
- Pediatric Planning
- Project Management
- Team Leadership
+5 more
Qualifications
- Bachelors Degree
- Graduate/Postgraduate (Preferred)
About Precision for Medicine
precisiongroupcompanies.comThe site is currently a placeholder that immediately redirects to /lander and contains no public content describing the company. Presuming it's a web-focused startup, it likely offers a SaaS platform to help businesses build high-converting landing pages and marketing funnels. Typical offerings would include a drag-and-drop page builder, A/B testing, analytics, and integrations with CRMs and email platforms to drive lead generation. Customers would be small-to-medium businesses and marketing teams seeking easy onboarding, template libraries, and conversion optimization tools.
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