Clinical Research Coordinator II

Benaroya Research•Seattle, WA

41d•$29 - $43

About The Position

Join a collaborative team at the Clinical Trials Unit of Benaroya Research Institute (BRI), where your work will directly support cutting-edge clinical research in partnership with Virginia Mason physicians. Our studies focus on a variety of specialties including Cardiology (treatment of either new medications or cardiac devices), Neurology, and Allergy studies. This role offers exposure to a wide range of clinical trials across various phases of development. You will be part of a supportive, team-oriented environment with unparalleled support from our physicians, clinic staff, and dedicated study teams. We are seeking a motivated and detail-oriented Clinical Research Coordinator (CRC) to support our Principal Investigators in executing high-quality research protocols.Schedule: Typically Monday through Friday from 8:00 AM to 4:30 PM, with a 30-minute lunch break. Work schedule may vary.

Requirements

Minimum of two years' experience is required.
Prefer higher education or vocational training specializing in healthcare.
Requires Medical Assistant, Phlebotomist and Medical Assistant, Registered licenses; licensure may be completed after hire.

Responsibilities

New study preparation, subject screening and recruitment, informed consent, subject history, adverse events, concomitant medication review, regulatory document filing, preparation for study monitor visits, test article (TA) handling, completion of case report forms, maintenance of source documents, proper standard or research billing, and ensuring site quality
Subject care requirements may include appointment scheduling, arriving, records review, treatment coordination, collecting vital signs, subject health assessment, and telephone triage/screening
The CRC will ensure protocol compliance and subject safety at all times
The CRC may also perform phlebotomy, specimen processing using universal precautions when appropriate and consistent with licensure; and participate in process improvement events as necessary
The CRC must maintain subject and document confidentiality at all times, understand and comply with the appropriate sponsor requirements, regulations including the Food and Drug Administration (FDA), Good Clinical Practice (GCP) and International Conference on Harmonization (ICH), Health Insurance Portability and Accountability Act (HIPAA), Institutional Review Boards, (IRB) and institutional policies and procedures
Requires knowledge of medical terminology and basic subject care
The ability to operate centrifuges and EKG machines is preferable
In addition, this position deals with increasingly complex studies, TA, disease, or earlier phase studies requiring increased depth of knowledge with all regulations, policies and procedures
In some instances, may provide guidance or informal supervision of a Research Assistant or Clinical Research Coordinator I in the conduct of their study