Experienced Statistical Programmer responsible for clinical trial programming at Johnson & Johnson. Focus on statistical programming, collaboration with clinical teams, and supporting data analysis.
Responsibilities
Complete and lead programming trial activities of low to medium complexity
Design and develop programs for clinical research analysis and reporting
Perform verification of programming and reporting activities
Review project requirements and documentation
Support submission activities for CDISC compliant data packages
Collaborate with team and cross-functional members
Ensure compliance with training and operational processes
Requirements
Bachelor’s degree or higher in computer science, data science, mathematics, public health, or relevant field
2+ years of relevant programming experience, preferably in Pharmaceutical, CRO or Biotech industry
Basic knowledge of programming processes and concepts
Understanding of regulatory guidelines (e.g. ICH-GCP)
Proficient in SAS and R for programming and data manipulation
Excellent written and verbal communication skills
Oncology and/or immunology experience preferred
Python experience preferred
Benefits
medical insurance
dental insurance
vision insurance
life insurance
short- and long-term disability insurance
business accident insurance
group legal insurance
retirement plans (pension and 401(k))
vacation time (120 hours per year)
sick time (40 hours per year)
parental leave (480 hours within one year of birth/adoption/foster care)
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