Hgr Specialist

IQVIA UK

United Kingdom
Site identification regulatory start-up
Site documentation review and negotiation
Investigative site primary point of contact
Executes feasibility, site identification, regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements

Job Summary

  • Executes feasibility, site identification, regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements.
  • Serves as the primary point of contact for investigative sites, tracking document completion and ensuring contracts are fully executed.
  • Performs tasks at a country/region level associated with site activation activities in accordance with applicable local and/or international regulations.

Matching Summary

Executes feasibility, site identification, regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements.

Skills & Requirements

Must-have

  • site identification regulatory start-up
  • site documentation review and negotiation
  • investigative site primary point of contact
  • track completion of appropriate documents
  • establish project timelines

Nice-to-have

  • advanced knowledge within a specific discipline
  • integrity in hiring process
  • zero tolerance policy for candidate fraud

Key Requirements

  • 1 - 3 years clinical research experience
  • 3 years healthcare environment experience
  • Bachelor's Degree Life sciences or related field

Work Rights

Not specified

Tailored Resume

Cover Letter