Clinical Research Coordinator II

Employment Type
Regular Full-Time
Requisition number
1791
Department
Clinical Research
Location : City
Seattle

Overview

Benaroya Research Institute at Virginia Mason (BRI) in Seattle, WA is an internationally recognized non-profit medical research institute affiliated with the Virginia Mason Health System.

The Clinical Trials Unit at Benaroya Research Institute works primarily with the physicians at Virginia Mason on Industry/Grant Funded studies that focus on their area of expertise. The main departments we work closely with are Neurology, Asthma/Allergy, Cardiology, and Rheumatology. Currently we are also working with the Infectious Disease department on COVID-19 protocols.

Responsibilities

The Clinical Research Coordinator II (CRC) performs increasingly complex tasks to facilitate clinical research, while providing service to Virginia Mason Physicians on their clinical trials specializing in Cardiology, Asthma/Allergy, Rheumatology, and Neurology. Strong communication and organization skills are required.

 

This position would offer a variety in studies that we conduct as well as the various phases of study development. Benaroya Research Institute and the Clinical Trials Unit encourage teamwork and collaboration. We have unparalleled support from our physicians, clinic staff and study staff.

 

The position includes: 

• 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
• Ensuring site quality

Subject care requirements may include appointment scheduling, records review, treatment coordination, collecting vital signs, subject health assessment, and telephone triage/screening. The CRC may also perform phlebotomy, specimen processing and participate in process improvement events as necessary.

Requirements

  • Two years of experience in clinical research is required. 
  • A Bachelor’s degree and SOCRA or ACRP certification is strongly preferred. 
  • May substitute a Masters degree in clinical research or related field or M.D. for the two years of clinical research experience.

All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, citizenship, disability or protected veteran status.

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