Csa Specialist

IQVIA

Copenhagen, Denmark
Hybrid
Site activation activities
Regulatory document management
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 and serving as the primary point of contact for investigative sites.
  • IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.

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 activities
  • Regulatory document management
  • Investigative site communication
  • Clinical trial processes knowledge
  • Fluent Danish and English

Nice-to-have

  • Strong organizational skills
  • Attention to detail
  • Ability to manage multiple priorities
  • Healthcare or clinical research background

Key Requirements

  • Bachelor's degree in Life Sciences
  • 1-3 years clinical research experience
  • Native or fluent Danish
  • Fluent English

Work Rights

Not specified

Tailored Resume

Cover Letter