Senior Clinical Research Coordinator – Translational Studies

Montgomery College

New York (NY)

Vor Ort

USD 75.000 - 110.000

Vollzeit

Vor 4 Tagen
Sei unter den ersten Bewerbenden

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Zusammenfassung

Vanderbilt Health is seeking a Clinical/Translational Research Coordinator III (CTRC III) to independently coordinate and manage clinical and translational studies, ensuring protocol compliance, data integrity, and participant safety. The role leads recruitment, oversees regulatory documentation, and supports study operations from initiation to closeout.

The candidate will manage communications among investigators, sponsors, and sites, monitor study performance, and ensure adherence to GCP and

Qualifikationen

  • Bachelor's degree and a minimum of three years of relevant experience.
  • Master’s training in Public Health preferred; prior research experience desired.
  • Proficiency in Microsoft Office applications and excellent organizational, time management, and project coordination skills.

Aufgaben

  • Lead STAR CRN studies and investigator‑initiated projects across all study phases.
  • Oversee startup activities: feasibility, planning, site readiness, timelines, and procedures.
  • Manage enrollment objectives, milestones, and reporting requirements to ensure timely completion.
  • Coordinate multi‑site activities, monitor performance, and ensure compliance with IRB, sponsor, and GCP standards.

Kenntnisse

Project coordination
Regulatory compliance
Data management
Microsoft Office
Communication

Ausbildung

Bachelor’s degree
Master’s in Public Health preferred

Tools

REDCap
MS Office

Jobbeschreibung

Vanderbilt Health is seeking a Clinical/Translational Research Coordinator III (CTRC III) to independently coordinate and manage clinical and translational studies, ensuring protocol compliance, data integrity, and participant safety. The role leads recruitment, oversees regulatory documentation, and supports study operations from initiation to closeout.

The candidate will manage communications among investigators, sponsors, and sites, monitor study performance, and ensure adherence to GCP and

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