• Perform discovery visits to access sites for research partnerships. • Complete nomination, qualification, and site activation submissions, visits, and reports. • Ensure site compliance with protocol. • Ensure high quality data collection by attending patient enrollments, key time point follow-up visits, and monitoring visits as appropriate. • Provide protocol and product/procedural training to clinical sites. • Assist sites with pre-screening patients to ensure appropriateness for clinical study, as applicable. • Provide procedural support to ensure safety of subjects in clinical studies. • Help with registries, new technology assessments, and other special projects as needed.