Brittanie Brockett

Directed three concurrent biological research programs valued at up to $2M, leading protocol development and multisite execution. Optimized flow cytometry, qPCR, and western blot assays, increasing reproducibility by 25% and sensitivity by 20%.

Coordinated three oncology research programs across three development sites, achieving a 95% reproducibility rate. Integrated automation into cell characterization workflows, reducing turnaround time by 10% and increasing data consistency by 15%.

Executed analytical workflows including ddPCR, gel electrophoresis, tape station, and RNA-seq to evaluate ten gene therapy candidates. Coordinated timelines and deliverables, improving project delivery times by 15%.

Supported EBOV vaccine and therapeutic development by conducting flow cytometry, PCR, ELISA, and cell-based assays. Authored and revised three SOPs, increasing operational efficiency by 10% and improving inspection readiness by 25%.

Led validation of new laboratory procedures and SEAP-based customer projects, managing timelines and resources. Performed ddPCR, EliSpot, flow cytometry, RNA extractions, and blood processing.

Managed laboratory operations, maintaining SOPs and coordinating equipment maintenance, reducing downtime by 20%. Conducted antibody neutralization, FRNT, plasmid purification, and cell culture activities.

Served as lead contact for six BSL4 program activities, coordinating workflows and supporting CDC inspection preparation. Executed vaccine and therapeutic evaluations across BSL2, BSL3, and BSL4 environments.

Performed high-throughput PCR using Hamilton robotics and manual workflows to support genetic testing programs. Maintained laboratory equipment and supported CAPA and deviation procedures.

Collected and processed specimens for toxicity screenings, ensuring accurate test ordering and documentation. Managed daily sample shipments and maintained sample integrity.

Executed multiple clinical study protocols by coordinating specimen collection and ensuring accurate data capture. Collaborated with healthcare professionals to assess patient eligibility and maintain documentation.

Pursuing a Master of Liberal Arts in Biotechnology, currently in progress.

Earned a Bachelor of Science in Biology with a minor in Chemistry.

Completed a Certificate of Regulatory Affairs in Medical Devices and Pharmaceuticals.

Completed the Regulatory Affairs Training Program.