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Clinical Research Coordinator III at UPMC

Pittsburgh, Pennsylvania, United States -

Full Time

Start Date

Immediate

Expiry Date

15 Dec, 25

Salary

0.0

Posted On

16 Sep, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Grant Applications, Manuscripts, IRB Applications, Research Papers, Data Collection, Study Recruitment, Staff Training, Team Meetings, Budget Monitoring, Supply Ordering

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 III prepares grant applications, manuscripts, and IRB applications while assisting with complex research papers. They also audit research studies, monitor budgets, and implement recruitment plans.