At Johnson & Johnson, I supported data and analytics deliverables for ongoing oncology clinical studies. I collaborated with stakeholders to translate study requirements into validated analytical outputs and supported data quality and regulatory workflows.
At Zifo RnD Solutions, I coordinated programming activities across five clinical trials as a Senior Programmer Analyst, including priorities, deliverables, timelines, and project risks. I also coordinated teams of four to five members and contributed to regulatory submission packages for four clinical studies.
Earlier at Zifo RnD Solutions, I used SAS and SQL to process, analyze, and report on clinical research data, including work supporting 10 oncology studies. I applied SDTM and ADaM standards and produced Tables, Listings and Figures in alignment with FDA and PMDA requirements.
My work has included clinical data validation, quality control, and regulatory documentation such as annotated CRFs, Define-XML, Reviewer’s Guides, and Analysis Results Metadata. I also delivered internal training on TLF development and programming processes.
