Miracle Doss Email & Phone Number

Jacksonville, Fl, Us

Jacksonville, Florida, United States

Managed a portfolio of 11 clinical studies (5 in development, 6 active) focused on Phase II-IV trials in pulmonary arterial hypertension (PAH), interstitial lung disease (ILD), chronic obstructive pulmonary disease (COPD), and idiopathic hypersomnia (IH), ensuring compliance with study protocols, GCP, and other regulatory guidelines.Collaborated with principal investigators, sub-investigators, and research staff to ensure smooth trial execution from start-up to close-out, coordinating patient recruitment, screening, informed consent, scheduling, and other study-related activities.Maintained accurate data through source documentation recorded in electronic databases; addressed discrepancies; ensured timely safety reporting; and managed study budgets, inventory, and vendor relationships.Prepared and submitted regulatory documents, amendments, and continuing review reports to the IRB while maintaining the investigator site file, delegation of authority logs, training logs, and all correspondence with the IRB and sponsors.Fostered relationships with cross-functional teams (nursing, pharmacy, lab, imaging) to ensure thorough execution of protocol activities from screening visits through end of treatment or early termination.Worked closely with internal and external stakeholders to monitor study activities, provide status updates, manage timelines, and meet deadlines.

Jacksonville, Florida, United States

Collaborated closely with hundreds of multidisciplinary research teams, principal investigators, and clinical research coordinators to execute clinical research projects aimed at advancing medical knowledge and improving patient care. Ensured strict adherence to ethical guidelines, regulatory requirements, and institutional review board (IRB) protocols for multiple studies throughout the entire clinical trial process. Followed standard operating procedures (SOPs) and research protocols to provide essential lab support services for biospecimen collections, accessioning, processing, storage, and shipment to support research objectives.Proficiently managed and organized patient data using good documentation practices and biorepository proprietary systems while maintaining strict confidentiality and ensuring data accuracy to monitor and document patient progress, adverse events, and study outcomes. Operated and maintained state-of-the-art laboratory equipment and technologies in CAP accredited laboratories crucial for various research studies, including advanced imaging and diagnostic tools to process whole blood sample collections. Worked with leadership on implementing and validating new specimen processing techniques, updating and editing standard operating procedures, and training new and returning colleagues on lab processes.

Charleston, South Carolina, United States

Followed standard operating procedures (SOPs) to operate appropriate machinery used to fill, assemble, weld, print, pouch, and pouch seal Endosafe® LAL Reagent Cartridges and packaging. Prepared Class 100 Cleanroom for production usage during the day by calibrating, testing, and troubleshooting machinery, rehydrating and testing appropriate raw materials, and loading the environmental chamber.Utilized Good Documentation Practices to maintain data integrity in batch records throughout production. Assisted in final packaging of Endosafe® LAL Reagent Cartridges and inspected pouches, printed product code, lot number, and expiration dates on pouches. Adhered to company’s quality policy by following appropriate gown donning and aseptic techniques to meet regulatory requirements, inspecting raw materials for any defects, and collaborating with Quality Control to properly troubleshoot quality issues.

Charleston, South Carolina, United States

Utilized Walgreens' proprietary computer program to access and manage prescription informationincluding patient prescriber data, drug selection, prescription interpretation, and insurance billing. Assisted with inventory management, including verification of quantities, storage, removal of outdated medications, andrestocking pharmaceuticals in short supply resulting in an increase of availability in COVID-19 supplies by 2%.Provided preventative health services including administration of COVID-19 vaccinations and Influenza vaccinations. Administered COVID-19 rapid tests and sample collection using proper aseptic and swabbing techniques per CDC guidelines.

Chicago, Illinois, United States

Employed aseptic techniques while working in controlled and classified environments, some of which required complete aseptic gowning increasing product quality by 5%. Complied with policies, Standard Operating Procedures, FDA current Good Manufacturing Practices, and any other government requirements. Assisted manufacturing supervisor to prepare reports related to machine hours, leaves of shop floor personnel, machine downtimes, productivity reports, and materials management