Research (Professional)

• 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