epidemiologist resume example with 8+ years of experience

Jessica Claire
, , 609 Johnson Ave., 49204, Tulsa, OK 100 Montgomery St. 10th Floor
Home: (555) 432-1000 - Cell: - - : - -

Pharmacist, proficient in Epidemiology, Pharmacovigilance, Drug safety and Scientific roles.

Possessing high level knowledge in leading public health initiatives in epidemiology, statistical data review, literature analysis, technical writing, disease surveillance and clinical research. With being forward-thinking and diligent, cross-functionally adept at managing concurrent objectives to promote efficiency and influence positive outcomes.


● Detailed information about human subject research.

● Basic knowledge of pharmacovigilance, regulations,risk management plans, aggregate safety reports, signal detection, clinical trials, and clinical development.

● Completed certifications about Bioethics, Bio specimen research and Human subject protection.

● Proficient using biostatistics software, SPSS,SQL,Tableau

● Good knowledge of GCP, IRB, FDA, SOP, AE, SAE, CRF, ICH, IND, and CRF guidelines.

● Quick and fast learner, adaptable to new work environment, and ability to prioritize task.

● Resourceful team-player with excellent interpersonal skills and an ability to build rapport with diverse groups.

● Professional and possess a high degree of urgency and self-motivation and have a strong work ethics.

● Possess a high degree of integrity and ability to maintain confidentiality with HIPAA guidelines, patient matters and other sensitive information.

11/2021 to Current
Epidemiologist Chenega Corporation Fort Eustis, VA,
  • Offered subject matter expertise for epidemiological research programs related to COVID-19 and other infectious diseases whilst maintaining continuous stringent safety levels and preventive measures to curtail spread
  • Implemented CDC and OSHA driven infection prevention and control policies to guide Medical departments.
  • Investigated clusters and outbreaks to identify source of infection, educating healthcare personnel regarding short and long term control measures.
  • Monitored procedures for medical staff regarding sterilization, disinfection and decontamination of personnel, instruments and equipment.
  • Consulted with local and state health departments to report infectious/notifiable cases.
  • Wrote reports outlining key health topics and response strategies.
07/2021 to 11/2021
Public Health Associate Baylor College Of Medicine Corpus Christi, TX,
  • Offered subject matter expertise for clinical assistance and program services on COVID-19 related issues, including contact tracing
  • Checked accuracy of public data and materials, making immediate changes upon discovery of outdated information, particularly with vaccines
  • Educated staff members on disease prevention, vaccines and mental health resources.
  • Assessed workplace compliance with key safety standards and government regulations, initiating remediation processes to correct deficiencies.
  • Answers over 50 calls per shift to answer questions and concerns about COVID-19 and other infectious diseases
02/2021 to 05/2021
Public Health Advisor Gap Solutions, Inc Us
, DC,
  • Spoke with health community workers and members of public about importance of health, prevention and treatment.
  • Enhanced public health initiatives by developing and improving materials.
  • Provided DHS (Department of Health Services) with corrective action plans.
  • Designed and coordinated health-centered training programs for the focused groups
  • Promoted public health initiatives through media collaborations, organization websites and press releases.
06/2016 to 06/2020
Pharmacovigilance Specialist Grifols Inc. Lancaster, CA,

Perform quality review for adverse events (AEs), serious adverse events (SAEs), and serious unexpected serious adverse reactions (SUSARs)

● Data entry of Individual Case Safety Reports (ICSRs) including general information, patient information, medical history, laboratory data, suspect drug, concomitant medications, and adverse event coding into Argus Safety Database and performing quality check of ICSRs

● Analyzed cumulative investigational and marketed product adverse event reports for inclusion in Periodic Safety Update Reports

Performing Safety Data entry in the database, Coding relevant Medical Terminology, Writing Narratives for MedWatch (FDA 3500A) and CIOMS forms for domestic and international cases

● Rehabilitated the loss of masticatory function through the fabrication of fixed and removable prosthesis such as crowns, bridges, implant crowns, RPD and complete dentures

● Research planning and execution including case studies and original research.

● Process case using MedDRA version 18 and have experience with MedDRA coding.

● Ensured accuracy of coding, which includes selecting appropriate event terms in MedDRA.

● Wrote narratives summarizing the events according to departmental SOPs for spontaneous and literature cases through assessment of all source documents.

● Reviewed, processed, coded, and submitted serious and non-serious adverse event reports for spontaneous and sponsored studies, in compliance with global regulations and compliance timelines.

● Prepared narratives for MedWatch (FDA 3500A) and CIOMS forms for domestic and international cases.

05/2012 to 12/2015
Drug Safety Associate Dr. Reddy's Laboratories Middleburgh, NY,
  • Reviewed orders from physicians for prescriptions, handled drug dispensing and answered questions from patients regarding medications.
  • Accurately enter adverse events data from individual case safety reports from both investigational and post marketing products.

● Interpret case-related information including medical conditions, lab results and procedures, as well as compile complete narrative summaries.

● Basic working knowledge of protocol design and details relating to the extraction and entry of SAE from clinical trials reports.

● Understanding of medical terminology and the ability to summarize medical information.

● Comprehensive knowledge of international drug safety and pharmacovigilance principles and regulations.

● Performs safety review of clinical trial protocols, investigator brochures, study reports, informed consent forms, and other study related documents for assigned studies.

Updated and entered appropriate data into Clinical safety database and ensured data was captured according to the verbatim.

Education and Training
Expected in 01/2012 to to
MPH: Epidemiology & Infection Control
University of Aberdeen - UK,
Expected in 06/2010 to to
Pharmacy: Pharmacy
University of Benin - Benin City,
  • Association for Project Management (APM)
  • Emergency Medical Responder (EMR)
  • COVID-19 Contact Tracer

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Resume Overview

School Attended

  • University of Aberdeen
  • University of Benin

Job Titles Held:

  • Epidemiologist
  • Public Health Associate
  • Public Health Advisor
  • Pharmacovigilance Specialist
  • Drug Safety Associate


  • MPH
  • Pharmacy

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