Precision for Medicine

Regulatory and Site Start Up Specialist

Precision for Medicine(13 days ago)

ChinaOnsiteFull TimeMedior$0 - $0Regulatory Affairs
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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.

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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
Precision for Medicine

About Precision for Medicine

precisiongroupcompanies.com

The 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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