-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

-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.

-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

-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

-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

⦁ 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