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Clinical Research Associate

Job in Coos Bay, Coos County, Oregon, 97458, USA
Listing for: Shriners Hospitals for Children
Full Time, Part Time position
Listed on 2026-01-01
Job specializations:
  • Healthcare
    Clinical Research, Medical Technologist & Lab Technician
  • Research/Development
    Clinical Research, Medical Technologist & Lab Technician
Job Description & How to Apply Below

Why consider this job opportunity:

  • All employees are eligible for medical coverage on their first day
  • 403(b) and Roth 403(b) Retirement Saving Plan with matching contributions of up to 6% after one year of service
  • Paid time off, life insurance, short-term and long-term disability available for full-time and part-time employees
  • Additional benefits include tuition reimbursement, pet insurance, and more
  • Recognized as the 2025 best mid-sized employer by Forbes
  • Opportunities for professional growth in a supportive learning environment
What to Expect (Job Responsibilities):
  • Coordinate and implement system-wide processes to standardize clinical research operations
  • Facilitate research activities through timely communication with various stakeholders and maintain daily operations of the clinical research management system
  • Manage and maintain Human Subjects and Regulatory documents for submission to the centralized Institutional Review Board
  • Work with study sponsors and agencies to obtain approval for clinical trials and research protocols
  • Provide education and support to research staff and ensure compliance with ethical and regulatory standards
What is Required (Qualifications):
  • Minimum of 3 years of clinical research experience (site management, study management, IRBs, and federal regulations)
  • Bachelor's Degree in clinical research, science, or a related healthcare field, or 5 years of relevant experience in clinical research administration
  • Extensive knowledge of clinical research processes and ethical standards
  • Ability to work collaboratively with investigators and research staff to ensure compliance
  • Commitment to human subjects' protection and ethical research practices
How to Stand Out (Preferred Qualifications):
  • Experience coordinating multi-site clinical studies
  • Job-related experience in oversight or performance management of human clinical studies
  • Familiarity with clinical research genomics and CLIA laboratory sample-processing workflows
  • CCRP or CCRC certification
  • Master's Degree in clinical research, science, or a related healthcare field

#Pediatric Care #Clinical Research #Career Growth #Employee Benefits #Ethical Standards

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Position Requirements
10+ Years work experience
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