At IQVIA RDS Pvt Ltd., I deliver SCR, OPS, incident, and validation support across clinical-study environments. I’ve progressed from project resource to deputy delivery lead and study owner.
I design, troubleshoot, and enhance SQL-driven study logic, including patient workflows, protocol amendments, randomization and enrollment rules, and capping alerts. I’ve independently completed 200+ OPS activities.
As an Associate Software Engineer, I supported development, configuration, debugging, unit testing, and operational maintenance of clinical IRT systems. My work included SQL scripts, stored procedures, study-table updates, and validation defects.
I also trained in clinical data handling, IRT systems, clinical trial workflows, and production support. I use data analysis, requirements gathering, and validation support to help teams deliver reliable work in regulated clinical environments.
