Rasha Alrifae

• Coordinate complex thoracic oncology clinical trial operations involving multidisciplinary teams including physicians, nurses, pharmacists, and sponsors.

• Lead regulatory compliance activities including SAE reporting, protocol deviation management, monitoring visits, and audit readiness.

• Optimize scheduling and workflow processes to ensure timely study execution and patient safety.

• Serve as a primary liaison between investigators, sponsors, and institutional departments to support efficient study operations.

• Supported clinical trials in pulmonary and sleep medicine, including collaborations with the CDC.
• Coordinated enrollment, patient tracking, and IRB documentation; ensured protocol and safety compliance.
• Maintained accurate records in REDCap and IHIS; verified medication and eligibility adherence.
• Integrated study procedures into clinical workflows through collaboration with providers and staff.

• Provided direct patient care support on a medical-surgical unit for over one year, assisting with daily living activities, mobility, vitals monitoring, and safety rounding in a high-acuity setting.
• Transitioned to the operating room environment for several months, supporting perioperative teams with room turnover, patient transport, and supply preparation.
• Collaborated with nurses, surgical techs, and physicians to ensure smooth care delivery and workflow efficiency.
• Documented care activities and vital signs in IHIS.

• Provided interpretation services in medical, educational, and state agency settings, with primary focus in healthcare.
• Supported clear, culturally sensitive communication in ERs, clinics, and surgical consults.
• Interpreted during complex discussions involving diagnosis, treatment, and discharge.
• Interpreted for Arabic-speaking high school students as part of contracted services for school districts.