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Clinical Research Coordinator

CEDENT

Scottsdale, AZ

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JOB DETAILS
SKILLS
Calendar Management, Calibration, Clinical Assessment, Clinical Research, Clinical Trial, Data Entry, Data Quality, Electrocardiogram, Establish Priorities, GCP (Good Clinical Practices), Online Recruiting, Organizational Skills, Phlebotomy, Research Protocols, Schedule Development, Site Initiation, Staff Training, Time Management
LOCATION
Scottsdale, AZ
POSTED
30+ days ago
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.

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