Clinical Study Coordinator

4 days ago


Oslo, Oslo County, Norway TN Norway Full time

About This Opportunity

TN Norway is offering an exciting opportunity for a skilled Clinical Research Associate to join our team. In this role, you will contribute to the success of our clinical trials by conducting site monitoring visits, managing subject recruitment, and ensuring protocol implementation.

Key Activities:

  • Conduct Site Monitoring Visits: Conduct on-site monitoring visits to ensure the quality and integrity of clinical trial data.
  • Develop Subject Recruitment Plans: Collaborate with study sites to develop and implement subject recruitment plans to enhance predictability.
  • Provide Protocol Training: Administer protocol training to assigned sites and establish regular lines of communication to manage ongoing project expectations and issues.
  • Maintain Study Documentation: Maintain accurate and complete documentation of study activities and results.

Requirements:

  • Education: High School Diploma or equivalent degree in scientific discipline or healthcare preferred.
  • Experience: Equivalent combination of education, training, and experience may be accepted in lieu of degree.
  • Skills and Knowledge: Basic knowledge of and skill in applying clinical research regulatory requirements (e.g., GCP and ICH guidelines).
  • Communication Skills: Excellent written and verbal communication skills.


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