Precision for Medicine

Regulatory and Start Up Specialist

Precision for Medicine(10 days ago)

RemoteFull TimeMedior$40,000 - $60,000Regulatory Affairs
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About this role

Precision for Medicine is a Clinical Research Organization specializing in precision medicine, oncology, and rare diseases. They are seeking a Regulatory and Start Up Specialist to support clinical trial site activation, ensure regulatory compliance, and facilitate communication with local authorities and sites. The role involves collaboration across various teams to prepare and manage documentation essential for clinical trial start-up activities.

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Required Skills

  • Regulatory Affairs
  • Clinical Trials
  • Document Management
  • Regulatory Submissions
  • Start-up Activities
  • GCP
  • IRB
  • Ethics Committees
  • Biomarkers
  • Data Analytics
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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