• Surveillance of multi-drug resistant (MDR) organisms and antibiotic resistance patterns in various healthcare settings in Maryland• Collect, review, analyze, and interpret surveillance data• Identify and lead investigations of MDR infectious disease outbreaks in various healthcare settings across different counties in Maryland• Collaborate with local health departments and healthcare providers across Maryland to prevent and manage multi-drug resistant infection outbreaks across healthcare settings• Update CDC and Maryland databases to track antibiotic resistance patterns and healthcare-associated infections• Recommend, coordinate, and implement appropriate infection prevention and control strategies in different healthcare facilities across Maryland• Perform contact tracing, including but not limited to patient chart review in CRISP and other EMRs• Educate and train healthcare providers on infection prevention and control measures• Develop SOPs for multi-drug resistance organisms(MDRO) surveillance and outbreak investigations in different healthcare settings

• Cataloged data and reported the results of samples while working in a team of 15 people• Developed patient data collection forms used for storage of baseline and follow-up data of study participants• Tracked patient enrolment and reviewed recruited patients for eligibility criteria • Managed clinical trial data entry and resolution of data quality inquiries• Identified and developed new methods for data entry and quality control measures to maintain data integrity• Completes proper patient sample processing and storage as outlined in the standard operating protocol• Ensured accurate data documentation in accordance with clinical research protocols• Mentored and coached five new staff on key laboratory processes through the probation period

Research work: The Association between Trace Elements and Coronary Heart Disease (CHD) among United States Adults • Designed the cross-sectional study from hypothesis formulation, research methodology, and data analysis to the result interpretation and presentation• Reviewed existing scientific literature • Imported relevant data of over 39000 study participants from the National Health and Nutrition Examination Survey (NHANES) website using the 2011 to 2018 cycles• Cleaned and merged the datasets obtained from the NHANES website using the SAS software while ensuring data quality control• Recoded variable names from imported datasets to standard codes for data analysis and use on other related research work by investigators at the practicum site• Analyzed data by the conduction of univariate and bivariate analysis, and building of logistic regression models using the SAS software• Communicated with practicum/internship supervisor all through the data analysis process• Visualized the results of the statistical analysis using tables and figures in scientific manuscript publication-quality• Documented the research methodology, data analysis, and results in a scientific manuscript• Presented research findings orally to the scientific audience at the department

•Provided essential clinical care to both acutely and chronically ill patients in outpatient and inpatient settings•Ensured accurate and consistent entry of medical history, drugs, and adverse events to ensure up-to-date patient record•Applied knowledge of pharmacokinetics and pharmacodynamics to review, investigate, and manage cases of reported adverse drug-related events• Led and coordinated internal cross-functional safety meetings, including scheduling, taking minutes, communicating, and sharing information (Safety Management Team and Executive Management meetings)• Compiled and analyzed results from all tests to determine the root cause of patients’ symptoms•Maintained and reviewed clinical documents (protocols, regulatory submission sections, clinical study reports, and presentations) for all patients•Facilitated responses to requests for safety information from health authorities•Complied with company procedures/Standard Operating Procedures (SOPs) and support updates to procedural documents as needed, especially relating to adverse drug event reporting and management

• Offered emergency, inpatient, and outpatient care for all patients with any form of medical illnesses• Collaborated with cross-functional departments to ensure timely communication of significant safety information• Ensured round-the-clock care for inpatients, especially those in the intensive care unit• Acted as a clinical research associate (CRA) for some clinical trials and conducted onsite drug safety monitoring of study participants• Created case notes and participated in both hospital and non-hospital-based research work• Updated patient medical records promptly and ensured confidentiality • Contributed to the formulation of the informed consent forms for various kinds of research• Ensured adherence to designed SOPs and compliance with prescribed medications• Supervised over 20 medical students and nursing staff on patient-centered care• Supervised other clinical operations carried out by newly employed physician interns

•Acquired extensive knowledge of all applicable SOPs, Clinical Practice (GCP), and health agency regulations and guidelines•Work closely with the Safety Physicians in planning, conducting, and evaluating Phase II, III, and IV trials•Ensured the accuracy and completeness of case reports by generating medical queries and communicating to corresponding investigational sites•Developed strong working relationships with colleagues, including but not limited to Clinical Safety Scientists, Clinical Directors in Clinical Research, Quality, Marketing, and Regulatory departments•Provided technical and scientific support to the Sr Medical Safety Physicians (MSP) in all activities related to signal detection, including analysis of safety data reports arising from post-marketing surveillance data and clinical trials•Reviewed line listings to detect safety signals and presented the reviews to the team

• Prepared educational materials and PowerPoint presentations for training/teaching year 3 and 4 medical students• Trained and guided over 50 medical students in preparing for the medical school’s Anatomy and Physiology medical examinations• Co-ordinated 11 laboratory sessions to facilitate understanding of essential seemingly complex concepts

• Prepared of educational materials and PowerPoint presentations utilized during meetings with potential sponsors to explain the benefits of the program, succeeding in winning 5 main sponsors• Designed educational materials and PowerPoint presentations with graphic illustrations to facilitate effective knowledge transfer and sensitization of over 100 participants• Liaised with Gynaecologists to conduct about 65 medical tests, mammograms, and pap smears to screen for cancer• Created 4 final reports summarizing program activities and achievements for media publication