Experienced Cra - Norway

IQVIA

Oslo, Norway
Perform site monitoring visits
Ensure study protocol adherence
Manage study progress
Perform monitoring and site management work to ensure sites conduct studies and report data as required by the protocol, regulations, and sponsor

Job Summary

  • Perform monitoring and site management work to ensure sites conduct studies and report data as required by the protocol, regulations, and sponsor.
  • Evaluate the quality and integrity of study site practices, manage study progress, and ensure proper documentation is maintained.
  • Collaborate with study team members and may support recruitment planning and site financial management.

Matching Summary

Perform monitoring and site management work to ensure sites conduct studies and report data as required by the protocol, regulations, and sponsor.

Skills & Requirements

Must-have

  • Perform site monitoring visits
  • Ensure study protocol adherence
  • Manage study progress
  • Maintain Investigator's Site File
  • Create study documentation

Nice-to-have

  • Drive subject recruitment plan
  • Collaborate with study team members
  • Effective time management skills
  • Problem-solving skills

Key Requirements

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

Work Rights

Not specified

Tailored Resume

Cover Letter