Clinical Research Coordinator (Scottsdale, AZ)
- 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
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