Over 10 years of experience in statistical programming for clinical trials, specializing in oncology, rheumatology, allergy & immunology, hematology & oncology, and schizophrenia. Expertise in CDISC standards (SDTM, ADaM), SAS programming, data analysis, and quality control processes for regulatory submissions. Strong leadership in project management, stakeholder communication, and technical innovation. Developed automation tools to enhance workflow efficiency and resource allocation.
SAS programming
Problem-solving abilities
Time management abilities
Project management
Statistical analysis
Multitasking