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Clinical Research Associate

3 weeks ago


Oslo, Oslo County, Norway TN Norway Full time
Job Overview

Clinical Research Associates are responsible for ensuring that clinical trials are conducted in accordance with Good Clinical Practice (GCP) and applicable regulations. The role involves performing site management tasks, monitoring study progress, and identifying potential issues.

Key Responsibilities:

  • Conduct site initiation visits to establish a relationship with the investigator and ensure they understand their responsibilities.
  • Perform regular monitoring visits to assess the quality of study conduct and identify any issues.
  • Collaborate with the study team to develop and implement corrective actions to address any issues identified during monitoring.
  • Evaluate the qualifications and experience of potential investigators and sites.
  • Develop and maintain documentation related to site management, monitoring, and regulatory compliance.

Qualifications and Experience:

  • Bachelor's degree in a scientific or health-related field.
  • Minimum 1 year of experience in clinical research, preferably as a CRA or SM.
  • Strong understanding of GCP and regulatory requirements.
  • Excellent communication and organizational skills.
  • Ability to work independently and collaboratively as part of a team.