Site Activation Specialist, Sponsor Dedicated (ra Expert)

IQVIA

Seoul, South Korea
Site identification and activation
Regulatory and start-up activities
Site documentation management
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.
  • Updates and maintains internal systems, databases, tracking tools, timelines, and project plans with accurate project-specific information.

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 and activation
  • Regulatory and start-up activities
  • Site documentation management
  • Investigative site point of contact
  • Contract negotiation with sites and sponsors

Nice-to-have

  • Collaboration with project management
  • Attention to detail in document review
  • Proactive communication with team members

Key Requirements

  • 1-2 years Regulatory Affairs experience
  • BA/BS degree in Life Sciences or related field
  • Proficient in English language

Work Rights

Not specified

Tailored Resume

Cover Letter