Regulatory and Site Start Up Specialist
Precision for Medicine(13 days ago)
About this role
Precision for Medicine is a contract research organization combining clinical trial execution with laboratory expertise and advanced data sciences, with a strong focus on oncology and rare disease. The Regulatory and Site Start Up Specialist is a country-based role (Shanghai/Beijing) supporting the company’s regulatory and site start-up operations for clinical trials.
Required Skills
- Regulatory Submissions
- Site Start-Up
- Informed Consent
- Document Review
- CA Interaction
- Budget Negotiation
- Project Tracking
- Translation Coordination
- TMF Maintenance
- Feasibility Assessment
Qualifications
- Bachelor’s Degree
- Registered Nurse (RN)
- MD
- PhD
- PharmD
- RAC
- Masters 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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