Regulatory and Start Up Specialist
Precision for Medicine(4 days ago)
About this role
The Regulatory and Start Up Specialist (RSS) is an experienced professional responsible for managing regulatory and site start-up activities related to clinical trials. They ensure compliance with local and international regulations, prepare submission documents, and support site activation and contractual processes.
Required Skills
- Regulatory Affairs
- IRB
- GCP
- Clinical Trials
- SOPs
- ICH Guidelines
- Contract Negotiation
- Document Management
- Regulatory Submissions
- Project Management
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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