Emily Brown Email & Phone Number

Reviewed IRB/EC-approved clinical trial consent documents in multiple eTMFs (Veeva, Phlex, ICON) for biospecimen testing.Interpreted compliant use and retention periods for biospecimens collected in clinical trials of all phases.Pinpointed complex biospecimen related consent permissions and categorized into pre-defined classifications based on country-specific regulations.Translated country-specific consent forms as needed.Communicated complex or ambiguous informed consent language for escalation and decision making by theclient team.Adapted to new projects in response to client requirements and deadlines.Completed intensive training on the entire clinical trial process, from startup to closeout, to support jobexecution.

Coordinated and monitored the entire lifecycle of oncology projects, from initiation to completion, and supported sourcing materials essential for projects.Primary point of contact for all questions and concerns from clients and other departments.Obtained CAP accreditation for the department by developing and adhering to current research standards.Supervised Biorepository staff and delegated daily tasks for seamless department operations.Evaluated patient eligibility for project participation utilizing EMRs and submitted follow-up data to researchersvia eCRFs such as OpenClinica.Ensured all site initiation activity including training checklists and documentation systems.Maintained regular communication with clients to provide status updates, performance metrics, and study-level feedback.Responded adeptly to changes in operating room schedules, patient consent refusals, and project closures as they occurred.Managed accurate documentation of biospecimen collections using Excel and BIMS.Performed weekly and monthly audits of department documents/specimen storage to ensure compliance anddevelop best practices.Contributed to QA/QC and utilization review committees to review project feasibility, consent design andenhance department practices.Fulfilled the responsibilities of a Medical Research Assistant as needed within the Biorepository setting.

Contributed to the department's foundational development by offering input on SOPs and researching required regulatory standards.Refined and adapted patient consent forms according to IRB standards.Archived former patient records and specimens for future research.Acquired consent from patients of all ages and backgrounds on a daily basis based on project needs and disease type.Thoroughly documented each stage of the collection process according to protocol, ensuring precise andtraceable specimen tracking in Excel and OpenSpecimen.Assisted as a point of contact for clients for collections.Ensured the shipment of biospecimens promptly and correctly following collections to clients.Conducted both wet and dry laboratory procedures as part of research protocols in the research domain.

Tampa/St. Petersburg, Florida Area

Provided laboratory support by washing glass/plastic ware, autoclaving, issuing lab coats, and etching glassware for research laboratories.Ensured the upkeep of TempTrak, ChemTrak, and BioRAFT systems.Customized a new website to promote departmental resources effectively.Engaged in collaboration with other Environmental Health and Safety (EHS) departmentmembers as required.Optimized the lab coat issuing process for research labs to enhance efficiency.

Bachelors Degree, Microbiology

High School Diploma

Activities and Societies: Orchestra