Abigail Lee Email & Phone Number

Rockville, Maryland, United States

Rockville, Maryland, United States

Rockville, Maryland, United States

Rockville, Maryland, United States

Ashburn, Va

⚬ Designed 5 office protocols to optimize the documentation and communication of 45+ office visits a day, resulting in the increase in accuracy of detailed records, patient compliance, and understanding of medical plan.⚬ Implemented the personally designed protocols throughout 3 offices in the Northern Virginia Area, which streamlined and boosted productivity within the office, especially for new team members. ⚬ Collect and processes over 45+ clinical laboratory specimens daily. Manages quality checks and assurances on clinical specimens according to guidelines set forth by third party laboratories. ⚬ Oversees the storage and shipment of clinical specimens. Manages the data entry and documentation of results.⚬ Triages 30+ incoming patient calls, screens for any adverse reactions to treatment regimens. Reports any severe or unforeseen adverse reactions to the provider that may fall out of the set clinical scope of practice and documents all interactions/information. ⚬ Extract and summarize medical history to communicate to providers and appropriate health departments. Document the clinical information for review. ⚬ Coordinate, review, and verify key clinical documents such as biologic therapy enrollment, informed consent (ICF), insurance approvals, and therapeutic drug delivery for approved use within the office.⚬ Communicate clinical/technical concepts to various members of the healthcare team and patients with varying levels of knowledge.⚬ Educates patients on office administrative and clinical procedures, answers any questions that arise. Obtains informed consent. ⚬ Cross-trained in scheduling, patient eligibility screening, and manages inventory for medical operations. Performs phlebotomy. ⚬ Research new dermatologic therapies via various medical platforms such as Up-to-date, etc.⚬ Manage and conduct new staff training through didactic presentations and hands-on laboratory approaches to increase protocol and work flow retention.

Centreville, Virginia

Provided clinical and technical support for the physician during medical and procedural cases. Maintained and organized office/medical resources necessary for daily operations.⚬ Constructed, systemized, and managed an electronic inventory system via Microsoft Excel/Word that eliminated unnecessary costs of over-purchasing resources.⚬ Performed EKG’s and intake of vital signs for pre-screening of patients for annual wellness checks. ⚬ Communicated and coordinated integral information in regards to medical insurance, patient status, and appropriate treatment plans between various members of the healthcare team.⚬ Forecast and oversaw supply purchases for medical (ie: vaccines/testing materials) and office use. ⚬ Performed all specimen testing and processing for analysis. Quality checks and assurance for specimens collected, cross checked for accuracy when shipped out to testing facilities. ⚬ Triage and collected vitals for the provider. Administered injections, EKGs, and other clinically relevant information prior to evaluation by the provider. Performed phlebotomy. ⚬ Cross trained in light medical billing, scheduling, and receptionist tasks.

Tampa, Florida

Research Assistant for Natural Products Research under Dr. Bill Baker at University of South Florida - Center for Drug Discovery and Innovation.⚬ Created presentations and presented findings at CASTLE conference to a wide audience including doctoral candidates, graduate students, undergraduate students, and spectators. Utilized the ability to synthesize complex information and present it to a more general audience with modern applications. ⚬ Assisted in the research and cross reference of novel compounds via various medical databases such as PubMed, ProQuest, International Pharmaceutical Abstracts (IPA), OVID, and Embase

Tampa/St. Petersburg, Florida Area

Research Assistant for Dr. Mark Goldman who was nationally funded by the National Institute of Alcohol Abuse and Alcoholism. ⚬ Collected and documented trial data for review and analysis using Microsoft Excel and SPSS. Responsible for maintaining trial-related essential documents.⚬ Conducted informed consent process and discussions with research participants, including answering any questions related to the study.⚬ Scheduled participants for screenings. Verified eligibility requirements.

Master Of Science - Ms, Physiology And Biophysics

Certificate, Advanced Biomedical Sciences

Bachelor Of Science - Bs, Biomedical Sciences, General

Activities and Societies: Phi Sigma Theta, Media Chair of the Vietnamese Student Association