I am a Clinical Research Training and Education Lead with experience overseeing FDA- and ICH-GCP–regulated clinical trials across multiple therapeutic areas, including cardiovascular disease, pulmonology, gastroenterology, obesity, neurology, and rare diseases. Throughout my career, I have managed study startup, participant recruitment and retention, regulatory compliance, investigator oversight, staff training, quality assurance, and sponsor interactions. I have successfully led research teams and collaborated with investigators, healthcare providers, sponsors, and CROs to ensure participant safety, protocol compliance, and data integrity. My experience includes developing recruitment and retention strategies, optimizing site workflows, and training clinical research professionals to improve study performance and operational efficiency. I am passionate about advancing clinical research through practical, patient-centered approaches that support successful enrollment, retention, and execution of high-quality clinical trials.

Sessions:

• From Budget to Bedside: Aligning Clinical Trial Finance with Operational Execution

• Research Team Member Recruitment, Retention, and Referrals: A Site Success Framework