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Clinical Research Coordinator III at UPMC

Pittsburgh, Pennsylvania, United States -

Full Time

Start Date

Immediate

Expiry Date

06 Feb, 26

Salary

0.0

Posted On

08 Nov, 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 Budgets, Recruitment Plans, Staff Training, Team Meetings, Auditing, Monitoring, Complex Problem Solving, 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 audit research studies, monitor budgets, resolve data collection issues, and implement recruitment plans.