Site Management Specialist

3 days ago


Oslo, Oslo County, Norway TN Norway Full time

Responsibilities and Requirements

The ideal candidate for this position will have a strong background in clinical research and excellent communication skills. Key responsibilities include:

  • Conduct Site Monitoring Visits: Conduct on-site monitoring visits to ensure the quality and integrity of clinical trial data.
  • Manage Subject Recruitment: Collaborate with study sites to identify and enroll suitable subjects for clinical trials.
  • Ensure Protocol Implementation: Ensure that study protocols are implemented correctly at study sites.
  • Maintain Regulatory Compliance: Ensure compliance with relevant regulatory requirements and industry standards.
  • Develop and Maintain Study Documentation: Maintain accurate and complete documentation of study activities and results.

Qualifications:

  • 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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