Hybrid Pulmonary Translational Trials Manager

The University of Pittsburgh

Pittsburgh (Allegheny County)

Ibrido

USD 85.000 - 120.000

Tempo pieno

24 ore fa
Candidati tra i primi

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Vantaggi offerti da questo lavoro

Flexible work from home

Descrizione del lavoro

The University of Pittsburgh is seeking a Regulatory Coordinator Leader to oversee clinical trials budgeting and regulatory documentation within the Pulmonary Translational Research Core. This role collaborates with principal investigators and project coordinators across affiliated hospitals and research sites to ensure compliant study conduct.

Responsibilities include drafting and submitting Pitt and external IRB protocols, budgeting for industry and government studies, managing trial

Competenze

  • Draft, submit and manage IRB protocols for Pitt and external boards.
  • Budget clinical trials for industry and government studies.
  • Coordinate regulatory documentation and trial budgeting with researchers.

Mansioni

  • Facilitate and oversee clinical trials and multi-site studies.
  • Direct day-to-day operations, manage resources and budgets.
  • Submit clinical trial applications and develop study procedures.
  • Draft, submit and manage protocols to Pitt and external IRBs.
  • Utilize electronic trial management systems (OnCore).
  • Coordinate with sponsors, auditors, monitors and IRB staff.
  • Support principal investigators and coordinators.

Conoscenze

Regulatory coordination
Budgeting
IRB submission
Clinical trials
Documentation management
Communication

Formazione

Bachelor's Degree

Strumenti

OnCore
Pitt IRB
Advarra

Descrizione del lavoro

The University of Pittsburgh is seeking a Regulatory Coordinator Leader to oversee clinical trials budgeting and regulatory documentation within the Pulmonary Translational Research Core. This role collaborates with principal investigators and project coordinators across affiliated hospitals and research sites to ensure compliant study conduct.

Responsibilities include drafting and submitting Pitt and external IRB protocols, budgeting for industry and government studies, managing trial

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