Pittsburgh, Pennsylvania, USA
25 days ago
Clinical Research Coordinator III

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.

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.

The University of Pittsburgh, Department of Neurological Surgery is recruiting for a Clinical Coordinator III.

As a Clinical Coordinator III, your duties include the following. Patient-Reported Outcome Measures (PROMs) Collection Administer PROMs to eligible study participants. Ensure accurate timely collection of patient-reported data. Maintain confidentiality ethical standards during data collection. Accurately enter collected data into research databases or electronic health records. Perform data quality checks ensure data integrity. Generate regular reports. Collaborate with grant managers to track and manage research funding. Assist in the preparation of grant applications progress reports. Ensure compliance with grant requirements budgetary guidelines. Assist in the preparation submission of IRB applications. Maintain up-to-date knowledge of regulatory requirements guidelines. Ensure research protocols are followed to maintain IRB approval. Handle the disbursement of compensation or incentives to study participants. Maintain accurate records of participant payments receipts. Comply with ethical standards regarding participant compensation. Coordinate logistics for research studies, including participant scheduling. Collaborate with healthcare providers to ensure study protocols are followed. Act as a point of contact for study-related inquiries from participants. Monitor manage the finances related to research studies. Track expenses, process invoices, and reconcile budgets. Assist in financial reporting to grantors stakeholders. Maintain organized secure records of study-related documents. Ensure all study documentation is current readily accessible. Assist with regulatory audits inspections.

Minimum education to be considered for this position is a master's degree in a related field.

Interested candidates, please go to Home | Talent Center: Careers at Pitt | University of Pittsburgh and use requisition #24008912 to apply for this position.

The University of Pittsburgh is an Affirmative Action/ Equal Opportunity Employer and values equality of opportunity, human dignity, and diversity, EOE, including disability/vets.

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