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Assist with administrative tasks for residency programs, including scheduling, payroll, event planning, and trainee onboarding while responding to inquiries.

The Study Coordinator II will coordinate clinical study visits, manage documentation, ensure compliance, facilitate subject recruitment, and perform biospecimen processing.

The Clinical Research Program Manager coordinates clinical trials, ensuring compliance with protocols, recruiting participants, and managing study data and communication.

The Project Coordinator supports the WIC Program by providing education and counseling on breastfeeding/chestfeeding, performs health assessments, manages record keeping, and trains site staff.