At IQVIA, I conducted centralized monitoring and subject-level reviews across clinical trials, assessing data quality and protocol compliance. I raised and tracked 1,000+ clinical data queries with study sites and study teams through resolution.
I identified discrepancies, protocol deviations, and potential subject- and site-level risks, and supported corrective and preventive actions. I also contributed to study management plans and worked with cross-functional teams to support data integrity, inspection readiness, and study timelines.
At Apollo Hospitals Enterprises Ltd., I reviewed oncology prescriptions and chemotherapy protocols for dosing, interactions, and medication safety. I also reported adverse drug reactions and counselled patients and caregivers on medication use and treatment adherence.
