Onsite Clinical Research Associate – Junior

Posted 3 hours ago

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About the role

  • Participate in the recruitment and retention phases of clinical trials
  • Conduct site visits, including site selection, initiation, monitoring, and close-out activities
  • Ensure compliance with ICH/GCP guidelines, SOPs (Standard Operating Procedures) and local regulations
  • Manage local study meetings and training sessions
  • Maintain study documentation and ensure accuracy
  • Support the quality management system and compliance with the Novo Nordisk Way and Business Ethics

Requirements

  • Prior experience as a Clinical Trial Assistant (CTA)
  • Solid experience as a research site coordinator
  • Knowledge of GCP (Good Clinical Practice)
  • Familiarity with EDC (Electronic Data Capture), IxRS and CTMS (Clinical Trial Management Systems)
  • Intermediate English
  • Recruitment and retention experience is desirable
  • Willingness to travel to research sites (≥ 50% of the time)

Benefits

  • Learning and development opportunities
  • Work in a global healthcare company that promotes long-term health

Job title

Clinical Research Associate – Junior

Job type

Experience level

Junior

Salary

Not specified

Degree requirement

Bachelor's Degree

Location requirements

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