
Rocio M
Clinical Scientist
Skills

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Work experience
ICON plc
Full-time • 3 yrs 1 mo
Clinical Data Monitoring Committee Lead
Mar 2025 - Present • 1 yr 6 mos
Ensures scientific rigor, patient safety, and protocol compliance across 15 clinical trials. Improved early detection of protocol deviations by 35% and reduced critical issue resolution time by 30%. Responsible for verifying IP dispensation, laboratory procedures, and eTMF completeness while managing query and deviation documentation to reduce turnaround time by 25%. Presents study status reports and risk assessments in sponsor meetings to improve trial transparency.
Biometric Project Associate
Jul 2023 - Feb 2025 • 1 yr 7 mos
Validated biometric data for 10,000 participants with 99.8% accuracy. Implemented quality controls that reduced data errors by 30% and discrepancies by 25%. Optimized review workflows to cut turnaround time by 25% and supported audits with zero non-compliance findings. Coordinated with cross-functional teams to ensure 100% on-time submissions and developed reports that increased out-of-scope issue detection by 18%.