This role supports clinical research operations by conducting study participant assessments, coordinating data collection, and ensuring accurate documentation in compliance with established SOPs and study protocols. The position collaborates with Contract Research Organizations (CROs), study sponsors, and project managers while screening and reviewing patient charts to support recruitment across multiple studies. Responsibilities also include maintaining regulatory compliance through adherence to IRB requirements, ensuring protocol integrity, and supporting quality assurance for all research-related activities.

Job duties include but are not limited to:
Conducts research assessments on study participants. which includes but is not limited to data collection, SOPs, developing source documents.
Engages with CROs for site reviews and annual monitoring visits.
Screens, communicates, and reviews Patient Charts for recruitment for multiple studies.
Not required but is preferred, phlebotomy training, and knowledge of collection of biopsy samples.
Keeps consistent documentation and communication with study sponsors and lead Project Managers.
Assists with and adheres to study protocols, and Institutional Review Board (IRB) renewal, modification, and approved protocols.
Ensures proper protocols are followed and quality assurance of research and related work.

A Bachelor's Degree is required for this position with at minimum one year of relevant experience

The University of Pittsburgh is an equal opportunity employer / disability / veteran.