Hybrid Senior Clinical Trial Director - Multi-Site

New York University

New York (NY)

Hybrid

USD 75.000 - 85.000

Vollzeit

Vor 4 Tagen
Sei unter den ersten Bewerbenden

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

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Zusammenfassung

New York University’s School of Global Public Health in New York, NY invites applications for the Clinical Trial Director role. The position leads a complex clinical trial across multiple hospitals and universities, planning, organizing, and performing high-level research activities.

The director will manage PI relationships, oversee budgets and regulatory compliance, develop trial protocols, coordinate conduct, prepare IRB submissions, analyze data, and mentor a research team.

Qualifikationen

  • Master’s degree or higher; DrPH/PhD preferred.
  • Minimum seven years of clinical research experience with increasing responsibility.
  • Ability to work independently with interaction with internal/external stakeholders.
  • Willingness to travel within the US.

Aufgaben

  • Plan, organize, lead, and perform advanced clinical research duties for a complex trial involving 12 hospitals and multiple universities.
  • Manage multiple Principal Investigator relationships and provide guidance on budget management and compliance.
  • Develop clinical trial protocols and submit documentation to IRB and regulators as needed.
  • Coordinate all aspects of clinical trial conduct and prepare IRB submissions for review and approval.
  • Oversee financial management, budgeting, and quarterly project account reviews.
  • Manage a team of research staff, including scheduling, workload, and performance.

Ausbildung

Master’s degree or higher
DrPH or PhD preferred

Jobbeschreibung

New York University’s School of Global Public Health in New York, NY invites applications for the Clinical Trial Director role. The position leads a complex clinical trial across multiple hospitals and universities, planning, organizing, and performing high-level research activities.

The director will manage PI relationships, oversee budgets and regulatory compliance, develop trial protocols, coordinate conduct, prepare IRB submissions, analyze data, and mentor a research team.

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