Regulatory & Start Up Specialist
Precision for Medicine(1 month ago)
About this role
The Regulatory and Start Up Specialist supports regulatory and site start-up activities for clinical trials within a CRO focused on rare diseases and oncology. The role contributes to ensuring study readiness and compliance with local and international regulations, coordinates with internal stakeholders and external authorities, and helps maintain program quality and inspection readiness.
Required Skills
- Site Activation
- CTA Preparation
- Regulatory Submissions
- CA Interaction
- EC Interaction
- Document Review
- TMF Maintenance
- Translation Coordination
- IMP Release
- Contract Negotiation
+5 more
Qualifications
- Bachelor's Degree in Life Sciences
- Registered Nurse (RN)
- Pharmacy Qualification
- MD
- PhD
- PharmD
- RAC Certification
- Master's in Regulatory Science
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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