Xiomara M.
Clinical Research Associate @Memorial Sloan Kettering Cancer Center
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WORK HISTORY
Clinical Research Associate @Memorial Sloan Kettering Cancer Center
New York, NY, US
Serve as primary liaison for six Phase Investigator-Initiated and industry-sponsored trials within Gynecologic Medical Oncology, overseeing activities from study startup through closeout.• Ensure protocol adherence by reviewing treatment plans in EPIC, monitoring compliance, and coordinating clinical procedures to align with protocol requirements.• Create and maintain pharmacogenetic sampling schedules, lab requisitions, and biospecimen workflows; coordinate external tissue sample procurement.• Lead study team meetings and PI communications by preparing agendas, taking detailed minutes, and driving follow-ups across regulatory, clinical, and data teams.• Manage cross-functional coordination to support patient scheduling, data quality, and regulatory documentation throughout the trial lifecycle.• Report study status, identify operational trends, and liaise with sponsors including AstraZeneca, Merck, Daiichi Sankyo, Eisai, and Summit Therapeutics.
EDUCATION
Brandeis University
Bachelor of Science - BS, Neuroscience and Biology
ABOUT XIOMARA M.
Clinical Research Professional with 4+ years of experience leading and supporting Phase I–IV trials across oncology, neurology, and cardiology. Skilled in coordinating site operations, maintaining regulatory compliance, and collaborating with sponsors and CROs to ensure high-quality study execution.Experienced across both academic and industry-sponsored settings, including Memorial Sloan Kettering Cancer Center and Mount Sinai, I bring a track record of improving enrollment, optimizing study workflows, and driving operational excellence.Passionate about advancing patient-centered science and bridging clinical and translational research. Committed to continuous learning, cross-functional collaboration, and long-term growth within the clinical development space.
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