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Clinical Research Coordinator at UPMC

Pittsburgh, Pennsylvania, United States -

Full Time

Start Date

Immediate

Expiry Date

22 Jul, 26

Salary

0.0

Posted On

23 Apr, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Grant writing, Manuscript preparation, IRB applications, Research auditing, Budget monitoring, Data collection, Protocol implementation, Staff training, Team leadership, Supply management

Industry

Hospitals and Health Care

Description

Prepares grant applications, manuscripts, Institutional Review Board (IRB) applications, research papers, and assists with complex research papers. Audits research studies, monitors study budgets, resolves complex data collection issues, and implements protocol-specific study recruitment plans. Trains staff and oversees student workers; leads team meetings. Monitors study budgets and orders supplies.

Responsibilities

The Clinical Research Coordinator prepares grant and IRB applications while managing research manuscripts and papers. They are also responsible for auditing studies, monitoring budgets, and overseeing staff and student workers.