Clinical Trials Coordinator: Research Ops & Compliance

UCLA Health

Los Angeles (CA)

Vor Ort

USD 79.000 - 128.000

Vollzeit

14 Tage+

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Zusammenfassung

UCLA Health in Los Angeles is seeking a Clinical Research Coordinator to manage the design, setup, conduct and closeout of clinical studies under supervision. The role includes coordinating multicenter trials and ensuring regulatory compliance with FDA CFR and ICH-GCP, collaborating with investigators, sponsors, and departments to support study administration.

The ideal candidate has a Bachelor's degree in a related field and 2+ years of experience in study coordination, with strong

Qualifikationen

  • Bachelor's degree and 2+ years of study coordination or clinical research coordination experience.
  • Ability to communicate effectively with students, staff, faculty and sponsors.
  • Strong organizational skills to manage regulatory files and deadlines.
  • Proficiency with Adobe and Microsoft Excel for daily tasks.

Aufgaben

  • Assist in design, setup, conduct and closeout of clinical studies under supervision.
  • Coordinate multicenter trials and ensure regulatory compliance with CFR and GCP.
  • Collaborate with PI, departments, sponsors and partners to support study administration.
  • Prioritize tasks and manage deadlines in a fast-paced environment.

Kenntnisse

Clinical research coordination
Multicenter coordination
FDA CFR compliance
ICH-GCP
Communication
Data management
Excel
Adobe Suite
Team collaboration
Prioritization

Ausbildung

Bachelor's degree in related area

Tools

Adobe
Microsoft Excel

Jobbeschreibung

UCLA Health in Los Angeles is seeking a Clinical Research Coordinator to manage the design, setup, conduct and closeout of clinical studies under supervision. The role includes coordinating multicenter trials and ensuring regulatory compliance with FDA CFR and ICH-GCP, collaborating with investigators, sponsors, and departments to support study administration.

The ideal candidate has a Bachelor's degree in a related field and 2+ years of experience in study coordination, with strong

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