Johnson & Johnson seeks an experienced statistical programmer to support clinical trial data analysis and reporting activities. The role involves designing and developing programs for clinical research, ensuring CDISC compliance, and collaborating with cross-functional teams on trials of low to medium complexity.
Responsibilities
Design and develop programs supporting clinical research analysis and reporting activities
Complete and lead programming trial activities with focus on quality and timely delivery of outputs
Verify programming and reporting activities; review project requirements and documentation
Create, verify, and deliver CDISC-compliant data packages and regulatory submission materials
Collaborate with programming team, data management, statistics, and clinical stakeholders on assigned projects
Requirements
Bachelor's degree in computer science, data science, mathematics, public health, or related scientific field
Approximately 2+ years of programming experience in pharmaceutical, CRO, biotech, or related industry
Proficiency in programming languages such as SAS, R, or Python for data manipulation and analysis
Basic knowledge of regulatory guidelines including ICH-GCP and clinical research concepts
Strong written and verbal communication skills
Familiarity with data structures and programming methods for statistical analysis
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