US - Coordinator II, Clinical Research

Shriners Children's•Portland, OR

About The Position

The Clinical Research Coordinator II (CRC) is a specialized, independent research professional responsible for oversight and compliance of system-wide and local Shriners Children’s clinical research activities. The CRC supports research in accordance with organizational policies and procedures, hospital regulations, the Code of Federal Regulations, and Good Clinical Practice guidelines, when applicable. The position works closely with the Chief of Staff, scientific and medical staff, and other research personnel to ethically recruit and consent vulnerable pediatric participants and appropriately collect and safeguard data. The CRC serves as the site’s primary liaison among research participants, local investigators, and study sponsors. The role focuses on proper study conduct, participant safety, and data quality and safeguards. The position reports to the Clinical Research Program Manager or local Hospital Administrator/Clinic Director and the Research Programs Office at SHC International Headquarters.

Requirements

  • At least 3 years of clinical research experience, such as site management, study management, IRBs, and federal regulations regarding clinical research compliance.
  • Without a bachelor’s degree, at least 5 years of specific job-related experience in clinical research administration.

Nice To Haves

  • Bachelor’s degree in clinical research, science, or another healthcare-related field.
  • Master’s degree in clinical research, science, or another healthcare-related field.
  • Experience coordinating intergroup or multi-site clinical studies.
  • CCRP or CCRC certification.

Responsibilities

  • Maintain contemporary knowledge of clinical research regulatory requirements and working knowledge of the clinical research process from protocol development through implementation.
  • Track all aspects of projects, including study, investigator, and IRB information, patient recruitment activity, and financial management.
  • Work with investigators, research leadership, study sponsors, and regulatory agencies to conduct clinical research and report results.
  • Coordinate data collection, statistical analysis, and dissemination of results throughout a clinical study.
  • Evaluate protocols for feasibility, including processes for data collection, entry, storage, and reporting.
  • Safeguard participants involved in research studies supported and approved by Shriners Children’s.
  • Facilitate local research programs and projects through collaborative, timely communication and teamwork.
  • Provide consultation and mentorship to site staff, residents, students, and volunteers on research processes, Good Clinical Practices, and clinical research regulations.
  • Coordinate research with other departments in a professional and timely manner.
© 2026 Teal Labs, Inc
Privacy PolicyTerms of Service