Benaroya Research Institute

Returning Candidate?

Clinical Research Coordinator I

Clinical Research Coordinator I

Type 
Regular Full-Time
Requisition Number 
2018-1476
Department 
Clinical Research

Responsibilities

A Clinical Research Coordinator I (CRC) 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. Such responsibilities may include:

 

  • 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
  • arriving
  • records review
  • treatment coordination
  • collecting vital signs
  • subject health assessment
  • telephone triage/screening
  • ensure protocol compliance and subject safety at all times 

Requirements

  • Requires good medical knowledge including medical terminology, and basic subject care.
  • May require phlebotomy and vital sign collection skills and the ability to operate centrifuges and EKG machines.
  • Prefer higher education or vocational training specializing in healthcare.
  • Minimum one year full-time related experience.

May require Healthcare Assistant Licensure Certificate or other specialized training.

 

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.