Csa Specialist

IQVIA

Denmark
Hybrid
Site activation and start-up
Regulatory and ethics submissions
Investigative site communication
The Site Activation Specialist is responsible for executing feasibility, site identification, regulatory, site start-up, and maintenance activities at the regional or country level

Job Summary

  • The Site Activation Specialist is responsible for executing feasibility, site identification, regulatory, site start-up, and maintenance activities at the regional or country level.
  • This role ensures compliance with applicable regulations, SOPs, and project requirements, preparing and managing site documentation.
  • The Site Activation Specialist serves as the primary point of contact for investigative sites and supports the establishment of project timelines and ensures contracts are fully executed.

Matching Summary

The Site Activation Specialist is responsible for executing feasibility, site identification, regulatory, site start-up, and maintenance activities at the regional or country level.

Skills & Requirements

Must-have

  • Site activation and start-up
  • Regulatory and ethics submissions
  • Investigative site communication
  • Clinical trial documentation management
  • Native or fluent Danish

Nice-to-have

  • Cross-functional team collaboration
  • Attention to detail
  • Managing multiple priorities

Key Requirements

  • Bachelor’s degree in Life Sciences or related field
  • 1-3 years clinical research experience
  • Fluent English (written and spoken)
  • Native or fluent Danish

Work Rights

Not specified

Tailored Resume

Cover Letter