Clinical Research Coordinator (Scottsdale, AZ) Job at CEDENT, Scottsdale, AZ

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  • CEDENT
  • Scottsdale, AZ

Job Description

The Clinical Research Coordinator is responsible for the coordination and administration of clinical trials under the direction and supervision of the Principal Investigator.
  • Carry out clinical trial activities by adhering to Good Clinical Practice and study protocols
  • Maintain the integrity of data while protecting the rights, safety, and well-being of patients enrolled in clinical trials
  • Perform phlebotomy, EKGs, and obtain vital signs
  • Work closely with study monitors to coordinate and carry out Site Qualification Visits, Site Initiation Visits, Interim Monitoring Visits, and Close-Out Visits.
  • Complete Feasibility Questionnaires with PI and reach out to pharmaceutical and device companies to participate in new studies
  • Communicate with Institutional Review Boards to maintain the proper oversight of clinical trials
  • Day-to-day oversight of the research team
  • Ensure research staff remains on task throughout the work day
  • Maintain a professional environment
  • Delegation and prioritization of tasks
  • Oversee recruitment of research studies in collaboration with the protocol specific CRCs and research assistants to ensure referrals are contacted within 24-hours and recruitment portals are maintained up-to-date
  • Manage batch shipment schedule Monday-Thursday based off of clinic and staff schedules
  • Work with protocol specific CRCs to ensure that binders are kept audit ready at all times
  • Ensure temperature controlled areas are maintained at the proper temperature and that temperature readings are documented daily upon arrival to the site
  • Ensure that Calibration Log is kept up-to-date
  • Ensure that research staff is following Research Task List in downtime
  • Manage the research calendar in accordance with Investigator schedules
  • Work with protocol specific lead CRCs to ensure that data entry and queries are attended to within a timely manner and per Clinical Trial Agreement timelines
  • Confirm that staff training is up-to-date at all times. Work with protocol specific CRCs to ensure that delegated staff trainings are up-to-date
**Please submit cover letter to be considered for this position.

Job Tags

Interim role,

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