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Quality Specialist

PanOncology Trials • San Juan, PR, US • published 2026-10-06 19:33:47.439695

Description

We are seeking a meticulous Quality Specialist to join our team. The ideal candidate will have prior clinical research experience. If you are detail\-oriented and passionate about maintaining high standards, we would like to hear from you! **Responsibilities:** * Protect the well\-being of research participants and comply with all regulatory guidelines and protocols as outlined in the research protocol and in accordance with federal, state and institutional policies. * Collaborate with investigators and statistical consultants, epidemiologists, research associates, regulatory staff, clinical research coordinators (CRC) and other relevant personnel in the execution of clinical research. * Collaborate with other departments to address quality issues and drive continuous improvement initiatives. * Submit reports, documentation and ensure all research protocol guidelines are followed. * Participate in research meetings and assist in coordination of specific meetings as required by the sponsor, the organization, the research compliance office and the leadership team. * Perform routine monitoring and quality audits of clinical trial documentation to identify areas of improvement. * Maint...

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