Jennifer O. Email & Phone Number

Atlanta Metropolitan Area

-Develops strong site relationships and ensures continuity of site relationships through all phases of the trial.-Adhere with corporate internal policies and requirements, including submission of timesheets and expense reports in a timely manner.-Interact with and guide study investigators and study coordinators in conducting clinical trials in accordance with study protocols. Member of a site Start-up Team for assigned projects

Greater Atlanta Area

-Conducted the recruitment and initial screening of potential subject's for a prospective multi-center randomized clinical trial.-Responsible for reviewing and collecting all of the subject''s medical history utilizing (EPIC) system.-Adhered to the patient''s care plan while ensuring 100% compliance with protocol requirements.-Exhibited excellent decision making skills in the management and administration of care to the specified patient population.

Atlanta, Georgia, United States

-Recruited and screened subjects for all assigned protocols within timelines.-Managed patient recruitment and retention strategies to meet enrollment goals and maintain participant engagement throughout the study duration.-Utilized Veeva Vault for the management of clinical trial documents, ensuring proper storage, version control and accessibility for study team members.-Monitored patient compliance with study protocols and facilitated follow up communication to ensure adherence to study requirements.-Properly consented subjects in accordance with FDA, GCP and protocol guidelines.-Scheduled all visits within proper time window set forth in the assigned protocols.Ensured subject safety in conjunction with the investigator-Assisted with quality assurance and tracked regulatory submissions.-Accurately recorded study data in source documents and case report forms

Atlanta, Georgia, United States

-Analyzed environmental samples for wet-chemistry, organic and in-organic compounds-Managed the preparation of sample spikes and surrogates, including extractions of unknown organic compounds-Increased Analytes recovery by 89% due to excellent laboratory techniques-Responsible for expedited delivery of a continuum of projects that enhanced the company’s delivery of analytical reports to its clients and received bonuses.-Developed new methods in the determination of total Phenolics, sulfides, alkalinity, acidity, turbidity and sulfates in ground water, drinking and saline waters which are still in use today

Conyers, Georgia, United States

-Suggested methods that helped in updating client profiles which resulted in an increase in sales.-Lead in the placing of orders for drugs and restocking of pharmacy shelves-Managed calls to patients, health care professionals and insurance companies-Communicated with physician’s offices to verify prescriptions and acquired refill authorizations-Ensured that patients understood the side effects and directions on their prescriptions-Track, document and periodically present status updates on active projects-Placed orders to restock the shelves and refill prescriptions-Perform computer entry of prescription information including patient search, prescriber search, drug selection, prescription interpretation and entry, insurance billing and problem resolution-Performed all functions and duties of a pharmacy service representative to ensure prompt service in the pharmacy department-Accept customer and prescription information required to process new and refill prescriptions, including refill authorization from doctor offices where permitted-Retrieve the appropriate medication form inventory where permitted-Create Prescription labels and put them on prescription containers where permittedPlace medication into prescription containers

Atlanta Metropolitan Area

⦁ Recruited and screened subjects for all assigned protocols within timelines.⦁ Properly consented subjects in accordance with FDA, GCP and protocol guidelines⦁ Oversaw all subject visits.⦁ Scheduled all visits within proper time window set forth in the assigned protocols.⦁ Ensured subject safety in conjunction with Investigator.⦁ Accurately recorded study data in source documents and case report forms.⦁ Design and maintained organizational tools to conduct the study accurately in Compliance with GCP, FDA and protocol guidelines

Masters Of Health Sciences In Clinical Research Administration, Translational Health Sciences, 3.5

Bachelor'S Degree, Analytical Chemistry, 3.70

Activities and Societies: NOBCChE