Clinical Research Coordinator III: Psychedelic Trials

University of Utah; Salt Lake City (UT); Vor Ort; USD 51.000 - 63.000; Vollzeit

Zusammenfassung

The University of Utah is seeking a Clinical Research Coordinator III to support a NIDA-funded trial on ketamine-assisted psychotherapy for opioid use disorder. You will coordinate daily trial activities, manage data and regulatory documentation, recruit participants, and ensure compliance with GCP and study protocols.

You will work with a team including study therapists, co-investigators, and the PI. Strong coordination and ethical conduct are essential for trial success and participant safety.

Qualifikationen

• Bachelor's degree and related work experience preferred.
• Experience in clinical research and Good Clinical Practice (GCP) knowledge preferred.

Aufgaben

• Coordinate and manage day-to-day clinical trial operations in accordance with GCP, study protocols, and regulations.
• Plan, organize, and implement complex study activities including visits, procedures, and follow-up.
• Collaborate with investigators, sponsors, teams, and regulatory entities on trial activities.
• Lead recruitment, screening, enrollment, and consent processes with ethical conduct.
• Maintain source documents, regulatory binders, and study records for audit readiness.
• Support pre-study activities and monitor visits, preparing materials and action items.
• Identify and report adverse events and protocol deviations per sponsor timelines.
• Oversee data collection, entry, and quality control; resolve data queries.
• Develop tracking tools to monitor milestones, enrollment, deadlines, and KPIs.
• Provide guidance and mentorship to junior staff; ensure best practices.
• Maintain participant-focused communication to support engagement and retention.

Kenntnisse

Clinical research coordination

GCP knowledge

Ausbildung

Bachelor's degree

Experience in clinical research

Jobbeschreibung

The University of Utah is seeking a Clinical Research Coordinator III to support a NIDA-funded trial on ketamine-assisted psychotherapy for opioid use disorder. You will coordinate daily trial activities, manage data and regulatory documentation, recruit participants, and ensure compliance with GCP and study protocols.

You will work with a team including study therapists, co-investigators, and the PI. Strong coordination and ethical conduct are essential for trial success and participant safety.