Alisha Proffitt

Coordinated Phase I oncology clinical studies, ensuring protocol, GCP, and FDA compliance through patient screening, visit scheduling, inclusion/exclusion validation, and timely source documentation. Managed laboratory sample collection and study medication dispensing, served as a liaison between caregivers and patients, and reported adverse events while maintaining strict confidentiality.

Supported clinical study operations as a Senior Clinical Research Coordinator by coordinating study activities and maintaining protocol-related documentation. Assisted the clinical team to ensure tasks were completed accurately and on schedule.

Coordinated clinical research activities as a Clinical Research Coordinator, helping manage study workflows and documentation. Supported accurate execution of protocol-required tasks to keep studies progressing.

Served as Lead Medical Transcriptionist, producing and reviewing clinical transcription for accurate documentation. Helped maintain documentation quality and confidentiality standards for patient records.

Provided medical scribing support as a Chief Medical Scribe to help ensure accurate and timely clinical documentation. Maintained confidentiality and documentation standards during patient encounters.

Worked as a Physician Scribe, supporting clinical documentation during patient visits. Contributed to accurate capture of patient encounter information while maintaining confidentiality.

Worked as an Emergency Room Scribe, providing support for accurate documentation during emergency department encounters. Maintained confidentiality and contributed to timely recording of patient information.

Served as an Emergency Room Scribe, supporting accurate clinical documentation during emergency department patient care. Ensured documentation was captured timely and maintained confidentiality.

Earned a Bachelor of Science in Biology at the University of North Carolina at Charlotte.