Career Opportunities

Clinical Research Associate

We are looking for an experienced Clinical Research Associate (CRA/Monitor) who would also be able to handle project management activities. Candidates must be able to work well with a global list of clients, international investigators, hospital ("site") staff and Nor Consult staff. This position requires that you work effectively in a multi-task environment and exhibit excellent communication, organizational and time-management skills. Travel may be up to 60% and may include international travel.

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Principal Duties and Responsibilities:

  • Conduct site visits including: Site Selection, Site Initiation, Interim Monitoring, Close-Out
  • Training site study staff on protocols (remote and on-site)
  • Review study data and work with site study staff to resolve data discrepancies
  • Assure protocol compliance
  • Manage assigned project deadlines
  • Prepare and review study documents
  • Ensure maintenance of study TMF and regulatory binders
  • Conduct in-house monitoring activities

Required Qualifications:

  • Minimum BA/BS or equivalent combination of education and work experience
  • Strong knowledge of US FDA regulations related to clinical trials, GCP guidelines
  • Ability to work independently, prioritize, and organize multiple projects
  • Highly organized and detail-oriented a must
  • Proficiency in computer skills - MS Office Suite (i.e., Word, Excel, Power Point, Outlook)

This is an office-based, full-time position. Our office is located in Tukwila, WA.

Please submit your resume to  for interest in the above career opportunity.