Responsibilities:During this job role, I manage day-to-day clinical research activities forsite, supervise clinical research staff, and ensure strict compliance withapplicable regulations and guidelines. I oversee and actively participate inexecution of all clinical research operations to ensure a streamlined dailyworkflow that delivers high-quality services in a coordinated and integratedmanner. I spearhead efficient and timely completion of regulatory documentsfor each study, overseeing entire process from startup to closeout andimplementing quality assurance measures. I enhance overall quality in clinicalresearch activities by evaluating, instituting, and executing new initiativesand processes.Key Achievements:● Cultivated robust business relationships with pharmaceutical companies,CROs, and IRBs, while serving as primary point of contact between members andsite.● Coordinated clinical research trials in accordance with protocol and GCPguidelines, recruiting study subjects to meet sponsor's goals and expectations.● Oversaw staff to ensure strict adherence to protocols and GCP guidelines,while actively participating in training initiatives to improve overall sitequality.● Initiated a diversity program aimed at accessing a more diverse populationfor clinical research participation.

Responsibilities:During this job role, I Collaborated with pharmaceutical companies, CROs, andinvestigators to conduct research studies efficiently and in compliance withregulations. Examined patient medical records, databases, and referrals toidentify research study candidates to ensure alignment with study protocolsand ICH/GCP guidelines for subject safety and study adherence. Applied studyprotocol and ICH/GCP guidelines rigorously to perform tasks such as collectingmedical history, vital signs, ECG, laboratory tests, and other study proceduresin accordance with protocol specifications. Elevated patient retention andsatisfaction during trial by cultivating an exceptional patient-providerrelationship.Key Achievements:● Developed and revised standard operating procedures in alignment with GCPguidelines and industry changes to ensure adherence to highest standards ofresearch conduct.● Successfully enhanced patient compliance throughout study duration byspearheading efforts to increase patient enrollment in clinical trials.● Improved diversity metrics at site by engaging and recruiting a more diversepopulation for participation in clinical trials.● Conducted training for new staff, contributing to improvement of dataquality and overall research effectiveness.● Optimized patient recruitment and retention strategies to ensure successof ongoing research initiatives.Career NoteClinical Research Coordinator, Florida Institute for Clinical Research –Orlando, FL (2020)Clinical Research Coordinator, Gutierrez Medical Center – Orlando, FL (2020)