Site Activation Specialist, Sponsor Dedicated (ra Expert)

IQVIA UK

Seoul, South Korea
Site identification and start-up
Regulatory and contractual document negotiation
Investigative site primary contact
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, managing documentation, contracts, and project timelines.
  • Requires advanced knowledge typically gained through extensive work experience and/or education in Life Sciences or a related field.

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 and start-up
  • Regulatory and contractual document negotiation
  • Investigative site primary contact
  • Site performance metrics tracking
  • Project timeline establishment

Nice-to-have

  • Collaboration with project teams
  • Attention to detail in document review
  • Adaptability to regulations and SOPs

Key Requirements

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

Work Rights

Not specified

Tailored Resume

Cover Letter