Worked independently to monitor and screen visitors and patients at Milstein Hospital and CHONY, abided by and enforced hospital policy in regards to COVID-19. Maintained stringent infection prevention techniques during the height of the COVID pandemic in NYC to protect patient and staff at the hospital.
Assisted nursing staff on various units at Milstein Hospital to deliver care to patients, obtaining vitals, assisting in ADLs and patient safety. Communicated and collaborated with medical and nursing staff to achieve quality healthcare outcomes for patients of varying levels of care. Maintained stringent infection prevention techniques during the height of the COVID pandemic in NYC.
Acted as regulatory authority and advisor by training and educating employees and advising leadership and PIs. Recruited, hired, and onboarded new Clinical Research Coordinators. Facilitated performance reviews.
Directly responsible for implementing a diverse portfolio of research activities for multiple studies. Recruited and trained CRCs in collaboration with leadership, mentored CRCs to help them successfully perform essential job functions. Created and implemented group specific training materials for new CRCs and Principal Investigators (PIs).
Executed multiple concurrent clinical research studies under guidance of protocols, UCSF and regulating agency policies. Oversaw data integrity, assured compliance with relevant regulatory agencies, and participated in external/internal audits or reviews of study protocols. Coordinated with other staff members and departments to facilitate study initiation, developed policies and procedures, assisted in training staff on new protocols, procedural changes, and other relevant procedures.
Collected clinical data for institutions retrospective prostate cancer database by examining and evaluating medical records. Collaborated with investigators and other study staff to manage prostate cancer research projects, including abstraction of medical information, completion of relevant IRB and regulatory paperwork. Consented patients to institute wide Cancer Research Study (Profile), collect and process fresh and archival tissue for study.
Conducted experiments with infants using eye tracking and EEG, recruited participants, maintained laboratory
schedule, completed literature searches and data interpretation protocols, trained new lab members each semester.