Clinical Research Coordinator I
Samaritan Health Services - Corvallis, OR
posted 7 months ago
About the position
The Clinical Research Coordinator I is responsible for coordinating and managing all aspects of clinical trials. This role involves coordinating and monitoring patient care while participating in clinical research studies. The coordinator will screen and evaluate patient eligibility, enroll participants, and monitor them to ensure compliance with study protocols. Additionally, the coordinator conducts study assessments and tests, assists in evaluating adverse events, and makes necessary dose modifications as required by the study protocols. The position is situated within the SHS Research Institute, which encompasses various departments including the Human Research Protections Program, Sponsored Program Administration, Clinical Research, Research Administration, and Research Development Offices. These departments collaborate to support research activities and secure external funding for SHS, which includes both sponsored and investigator-initiated research as well as quality improvement projects at all stages. The overarching goal of the Research Institute is to foster a culture of scholarly inquiry and promote data-driven discoveries that align with Samaritan's mission of enhancing community health.
Responsibilities
- Coordinate and manage all aspects of clinical trials.
- Monitor patient care while participating in clinical research studies.
- Screen and evaluate patient eligibility for clinical trials.
- Enroll patients and ensure protocol compliance throughout the study.
- Conduct study assessments and tests as required by the protocol.
- Assist in the evaluation of adverse events and make dose modifications as necessary.
Requirements
- Associate's degree in a health or science related field or equivalent experience.
- CMA/RMA certification plus one year of experience in a similar role.
- Completion of college coursework in science or healthcare education.
- Experience or training in computer applications including Microsoft Word, Excel, and Outlook.
- Healthcare Provider Level BLS certification required within 60 days of hire.
- Clinical Research Certification (CCRC, CCRA, or CCRP) required within four years of hire.
- Experience in healthcare is preferred.
- Experience or training in clinical research is preferred.
Nice-to-haves
- Experience in a clinical research setting.
- Advanced knowledge of medical terminology and procedures.
- Familiarity with electronic data capture systems.
Benefits
- Competitive hourly wage ranging from USD 19.52 to 28.67.
- Full-time employment with potential for career advancement.
- Access to continuing education and professional development opportunities.
