
Dynamic research and medical professional with proven expertise in clinical research and data management at Elligo Health Research. Skilled in teamwork and documentation, I enhance patient care through effective communication and meticulous attention to detail, ensuring compliance with protocols and optimizing study processes for improved outcomes.
Develop strong working relationships and maintain effective communication with study team members, assist with the screening, recruiting and enrollment of research subjects, perform patient/research participant scheduling, collect patient/research participant history, data entry and management, coordinate follow-sup care and laboratory procedures, Support the collection and review of required essential study documents and reports.
Order supportive study supplies (e.g., contracts, IXRS, lab kits, non clinical supply materials, imaging and laboratory handling manuals, etc.), adhere to an IRB approved protocol, assist in the informed consent process of research subjects, support the safety of research subjects, coordinate protocol related research procedures, study visits, and followup care, comply with clinic, and sponsor policies, standard operating procedures (SOPs) and guidelines, schedule subject visits and procedures, duties as assigned by study team lead/leadership
BLS certification