Hgr Specialist

IQVIA Inc

Site identification regulatory
Start-up and maintenance activities
Site documentation management
Executes feasibility, site identification, regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements at the regional or country level

Job Summary

  • Executes feasibility, site identification, regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements at the regional or country level.
  • Serves as the primary point of contact for investigative sites, tracks completion of appropriate documents, ensures contracts are fully executed, and establishes project timelines.
  • IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.

Matching Summary

Executes feasibility, site identification, regulatory, start-up, and maintenance activities in accordance with regulations, SOPs, and project requirements at the regional or country level.

Skills & Requirements

Must-have

  • site identification regulatory
  • start-up and maintenance activities
  • site documentation management
  • negotiate site documents and contracts
  • track site performance metrics
  • primary point of contact for sites

Nice-to-have

  • advanced knowledge within discipline
  • honesty and professionalism

Key Requirements

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

Work Rights

Not specified

Tailored Resume

Cover Letter