Clinical Research Coordinator I-II

Employment Type
Regular Full-Time
Requisition number
1765
Department
Clinical Research
Location : City
Seattle

Overview

The Clinical Research Program at the Benaroya Research Institute at Virginia Mason (BRI) is committed to giving patients access to clinical trials.  Working with clinicians at Virginia Mason Franciscan Health (VMFH), the Clinical Research Program at BRI differentiates itself by focusing on patient-centered research.  BRI is an independent, non-profit organization with a culture based on the values of collaboration, respect, innovation and inquiry.  Team members work together to support patients and clinicians with the goal of better outcomes for all.

 

Visit BenaroyaResearch.org or follow BRI’s Autoimmune Life BlogFacebookInstagram, 
LinkedIn or Twitter to learn more.

 

A Clinical Research Coordinator (CRC) I-II performs an increasing complexity of tasks to facilitate clinical research which may include working with affiliate or collaborating research sites as well as conducting BRI based research studies. This position is based in the Cancer Clinical Research Unit, with patient visits occurring in the downtown Seattle Virginia Mason outpatient oncology clinic. The CRC I-II will manage a variety of oncology trials in Phases I – III. This position functions as part of a highly dynamic team of Coordinators and Research Assistants (RA), and requires the candidate to be on-site a majority of the time.  

Responsibilities

  • Subject screening and recruitment
  • Informed consent
  • Subject history
  • Adverse events
  • Concomitant medication review
  • Medical records review
  • Planning and coordination of study visits
  • Supporting Principal Investigator in the conduct of trials
  • Regulatory document filing
  • Preparation for study monitor visits
  • Test article (ta) handling
  • Completion of case report forms
  • Maintenance of source documents
  • New study document preparation and planning
  • 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, shipping, and/or storage, 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 Practices (GCP’s) and International Conference on Harmonization (ICH), Health Insurance Portability and Accountability Act (HIPAA), Institutional Review Boards, (IRB) and institutional policies and procedures.

Requirements

Clinical Research Coordinator I

  • Minimum one year full-time related experience
  • Prefer higher education or vocational training specializing in healthcare
  • Requires good medical knowledge including medical terminology, and basic subject care
  • May require Healthcare Assistant Licensure Certificate or other specialized training

 

Clinical Research Coordinator II

  • 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 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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