Monitor and manage clinical trials, ensuring compliance with protocols and regulatory requirements. Conduct site visits, verify data accuracy, and train site staff on procedures while maintaining effective communication with stakeholders.

Manage clinical trial preparation and participant recruitment, oversee data management and protocol integrity, and coordinate multiple clinical sites while contributing to the research team's mission and disseminating innovative healthcare solutions.

Coordinate pediatric clinical study activities, manage data entry and electronic systems, assist in protocol development, and ensure compliance with research regulations while collaborating with multiple departments and stakeholders.

This role provides leadership for a centralized human biospecimen program, overseeing the development and implementation of policies and procedures to ensure ethical acquisition, use, and distribution of biospecimens in compliance with regulations. The administrator also serves as the Institutional Stem Cell Research Oversight (ISCRO) Administrator, supporting ISCRO activities and managing committee operations, including the Biospecimen Transfer Committee (BTC).