The Product Owner defines product direction and manages the product backlog to support NMDP's mission through iterative delivery. They act as a bridge between business and technology, collaborating with stakeholders to prioritize features and ensure high-quality solutions.
Provide independent quality and regulatory oversight of computerized systems and digital solutions through audits, documentation reviews, risk assessments, and compliance evaluations. Partner with IT, quality, product, system, and process owners to strengthen governance, assess suppliers and changes, and support investigations and corrective actions.
This role provides leadership and direction to the Donor Engagement functional area, ensuring the effective education and processing of potential transplant donors. The manager is responsible for team performance, process optimization, and maintaining high standards of quality and regulatory compliance.
The Donor Engagement Specialist is responsible for contacting and engaging potential donors to facilitate the life-saving donation process through effective communication and investigative research. The role involves managing donor records, conducting health screenings, and coordinating logistics such as laboratory testing and kit distribution.
The specialist engages with donors on the NMDP registry to confirm interest, assess health conditions, and coordinate the donation process. They manage donor records, conduct health screenings, and maintain professional relationships with internal and external stakeholders.
The Donor Engagement Specialist is responsible for contacting and engaging potential donors on the NMDP registry to facilitate the life-saving donation process. This includes conducting health screenings, coordinating laboratory testing, and maintaining accurate donor records within internal systems.
The Donor Engagement Specialist is responsible for contacting and engaging potential donors on the NMDP registry to facilitate the life-saving donation process. This includes conducting health screenings, coordinating laboratory testing, and maintaining accurate donor records within the database.
Independently conduct remote and on-site monitoring for multicenter clinical studies, including source verification, regulatory document review, site compliance assessment, issue resolution, and reporting. Manage site operations and study tracking, support investigators and study teams, lead centralized monitoring activities, and train junior CRAs.
The Senior Clinical Research Associate leads multi-center clinical research studies, performing site monitoring visits and ensuring compliance with protocols and regulatory standards. They also provide mentorship to junior team members, manage study metrics, and oversee site activation and data reporting processes.
