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PV & Regulatory Affairs Officer at New Country Healthcare LLC.
London, London - England, United Kingdom -
Full Time

Start Date

Immediate

Expiry Date

03 Jan, 27

Salary

50000.0

Posted On

05 Oct, 26

Experience

3 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Yes

Skills

Industry

Pharmaceutical Manufacturing

Description
  • Organize and deliver study metrics, reports, and tracking (site activation, enrollment, monitoring visits)
  • Coordinate meetings, prepare agendas, presentations, and meeting minutes
  • Support study document reviews (ICFs, CRFs, study manuals, reference binders)
  • Maintain Trial Master File (TMF) reconciliations and support regulatory/registry postings
  • Manage SharePoint/shared drive sites and track key study documents (1572s, financial disclosures, etc.)
  • Contribute to site feasibility, training materials, and close-out activities
  • Proactively identify process improvements and support Third Party Vendor oversight
Responsibilities