Sr. Site Activation Coordinator

IQVIA

Slovakia
Site activation activities
Regulatory compliance
Document review
The role ensures timely and compliant site start‑up activities in line with applicable regulations, SOPs, project requirements, and contractual or budgetary guidelines

Job Summary

  • The role ensures timely and compliant site start‑up activities in line with applicable regulations, SOPs, project requirements, and contractual or budgetary guidelines.
  • Prepare and review site documentation for completeness, accuracy, and consistency.
  • Maintain accurate study information in internal systems, databases, trackers, and timelines.

Matching Summary

The role ensures timely and compliant site start‑up activities in line with applicable regulations, SOPs, project requirements, and contractual or budgetary guidelines.

Skills & Requirements

Must-have

  • site activation activities
  • regulatory compliance
  • document review
  • data management

Nice-to-have

  • strong attention to detail
  • organizational skills
  • work independently
  • handling non-routine tasks

Key Requirements

  • Bachelor’s degree in Life Sciences
  • Experience in clinical research environment
  • Good knowledge of MS Office

Work Rights

Not specified

Tailored Resume

Cover Letter