At St Jude Children's Research Hospital, I oversee the safety and integrity of data in high-risk clinical trials. I coordinate monitoring activities with the External Data Safety Monitoring Board, investigators, and biostatisticians, and orchestrate biannual DSMB meetings.
At University of Tennessee Health Science Center (UTHSC), I reviewed human subject research protocols and submissions, provided regulatory and ethical guidance, and trained research teams on the IRB process and iMedRIS.
Earlier, I coordinated clinical research nursing at Northwestern University Feinberg School of Medicine, Moffitt Cancer Center, and Rush University Medical Center. My work included participant recruitment and informed consent, study visits, safety reporting, and regulatory documentation across infectious disease, pulmonary, and oncology studies.
