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Benaroya Research Institute · 1 month ago

Clinical Research Coordinator I/II

Seattle, WA

Full-time

Onsite

Entry, Mid Level

$24.67/hr - $35.78/hr

1+ years exp

Benaroya Research Institute (BRI) is a nonprofit research institute that collaborates with Virginia Mason Medical Center to support clinical research. The Clinical Research Coordinator will assist Principal Investigators in executing high-quality research protocols and will be involved in various phases of clinical trials across multiple specialties.

Clinical TrialsHealth CarePharmaceutical

Responsibilities

Facilitate clinical research, including collaboration with affiliate or partnering research sites and conducting BRI-based studies

Prepare for new studies, including regulatory document filing and study monitor visit preparation

Screen and recruit study subjects, obtain informed consent, and document subject history

Review adverse events, concomitant medications, and ensure protocol compliance and subject safety

Handle test articles (TA), complete case report forms, and maintain source documents

Manage proper standard or research billing and ensure site quality

Coordinate subject care, including appointment scheduling, record reviews, treatment coordination, and health assessments

Collect vital signs, perform telephone triage/screening, and assist with subject arrivals

Conduct phlebotomy, specimen processing using universal precautions, and other procedures as appropriate

Participate in process improvement activities and develop corrective and preventive action plans

Qualification

Clinical research experienceClinical Practices (GCP)FDA regulationsPhlebotomy skillsMedical terminologyProcess improvementHealthcare licensureInformal supervisionTeam collaborationSubject confidentiality

Required

Minimum of one year full-time related experience required for Clinical Research Coordinator I

Minimum of two years full-time related experience in clinical research required for Clinical Research Coordinator II

Must maintain subject and document confidentiality at all times

Understand and comply with sponsor requirements, FDA regulations, Good Clinical Practices (GCP), International Conference on Harmonization (ICH), HIPAA, IRB, and institutional policies and procedures

Requires good medical knowledge, including medical terminology and basic subject care

May require phlebotomy and vital sign collection skills, as well as the ability to operate centrifuges and EKG machines

Ability to provide guidance or informal supervision to a Research Assistant or CRC I in the conduct of their study, as applicable