Experienced Cra - Norway

IQVIA UK

Norway
**
Good clinical practice (gcp) knowledge
International conference on harmonization guidelines
Site monitoring visit execution
** IQVIA UK is seeking an Experienced Clinical Research Associate (CRA) to perform monitoring and site management in Norway. Candidates should have at least two years of on-site monitoring experience and a relevant degree, with strong organizational and communication skills. **

Job Summary

  • The role involves performing site monitoring visits to ensure studies are conducted according to the protocol and regulations.
  • Candidates must manage subject recruitment plans and maintain accurate documentation for the Trial Master File.
  • IQVIA is a leading global provider of clinical research services committed to accelerating medical treatment development.

Matching Summary

Match Score: 75

** IQVIA UK is seeking an Experienced Clinical Research Associate (CRA) to perform monitoring and site management in Norway. Candidates should have at least two years of on-site monitoring experience and a relevant degree, with strong organizational and communication skills. **

Skills & Requirements

Must-have

  • Good Clinical Practice (GCP) knowledge
  • International Conference on Harmonization guidelines
  • Site monitoring visit execution
  • Subject recruitment plan tracking
  • Trial Master File maintenance

Nice-to-have

  • Strong problem-solving skills
  • Effective time management abilities
  • Local language proficiency in Norway
  • Financial management of clinical trials

Key Requirements

  • Bachelor's Degree in scientific discipline or health care preferred
  • At least 2 years of on-site monitoring experience
  • Proficiency in Microsoft Word, Excel, and PowerPoint
  • Good command of English and local language

Work Rights

Not specified

Tailored Resume

Cover Letter