Tecnical Summary; New Protocol & Risk Review: Conducts in-depth, independent pre-reviews of complex, high risk biomedical, clinical, and socio-behavioral research protocols, including consent form documents and determinations (e.g., research vs non-research). Evaluates ethical considerations and assesses risks and benefits, particularly for vulnerable populations. Reliance & Single IRB (sIRB): Leads reliance agreement negotiations, manages external IRB partnerships, and coordinates multi-site communication strategies ensure regulatory alignment and compliance. Investigator Support and Consultation: Serves as a resource to Principal Investigators and study teams, providing expert guidance on new protocol submissions, informed consent language, and cede review reliance process .Post-Approval Monitoring: Supports the continuing review and modification process and evaluates unanticipated problems

Job Summary:

Leads the development, revision, implementation, and communica...