Senior Ketamine Trial Coordinator

University of Utah Health Research

Salt Lake City (UT)

Vor Ort

USD 51.000 - 63.000

Vollzeit

Vor 2 Tagen
Sei unter den ersten Bewerbenden

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

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Zusammenfassung

University of Utah Health Research is seeking a Clinical Research Coordinator III to support a NIDA-funded ketamine-assisted psychotherapy trial for opioid use disorder. The role involves coordinating day-to-day trial activities, ensuring GCP compliance, managing study visits, consent, adverse events, data entry, and regulatory documentation, and collaborating with a multidisciplinary team.

Prefer candidates with experience in substance use disorders or vulnerable populations; the position

Qualifikationen

  • Equivalency: 1 year of higher education substituted for 1 year of related work experience.
  • Clinical Research Coordinator (Non-R.N.), III requires a bachelor’s (or equivalency) + 6 years or a master’s (or equivalency) + 4 years of related work experience.

Aufgaben

  • Coordinate and manage day-to-day clinical trial operations in compliance with GCP, protocols, and regulations.
  • Plan, organize, and implement complex study activities to meet protocol objectives, including visits and required follow‑ups.
  • Lead participant recruitment, screening, enrollment, and informed consent processes with ethical conduct and safety.
  • Maintain source documents, regulatory binders, and study records; ensure audit readiness.
  • Develop tracking tools to monitor milestones, enrollment, deadlines, and KPIs; provide regular updates to investigators.

Ausbildung

Bachelor’s degree or higher (or equivalent)

Jobbeschreibung

University of Utah Health Research is seeking a Clinical Research Coordinator III to support a NIDA-funded ketamine-assisted psychotherapy trial for opioid use disorder. The role involves coordinating day-to-day trial activities, ensuring GCP compliance, managing study visits, consent, adverse events, data entry, and regulatory documentation, and collaborating with a multidisciplinary team.

Prefer candidates with experience in substance use disorders or vulnerable populations; the position

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