Site Activation Coordinator

IQVIA

Multiple Locations
Fully remote
Site identification and activation
Regulatory and start-up activities
Site documentation management
Executes feasibility, site identification, regulatory, and start-up activities in accordance with regulations, SOPs, and project requirements

Job Summary

  • Executes feasibility, site identification, regulatory, and start-up 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.
  • Updates and maintains internal systems, databases, tracking tools, timelines, and project plans with accurate project-specific information.

Matching Summary

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

Skills & Requirements

Must-have

  • Site identification and activation
  • Regulatory and start-up activities
  • Site documentation management
  • Investigative site communication
  • Project timeline establishment

Nice-to-have

  • Pivoting to site activation
  • Learning new things
  • Zero tolerance for fraud

Key Requirements

  • Bachelor's Degree Life sciences or related field
  • At least 1 year clinical research experience
  • Advanced level of English

Work Rights

Not specified

Tailored Resume

Cover Letter