Experienced I Stat Programmer
Johnson & Johnson
Overview
In this role, you develop, verify and document statistical programs to analyze and report clinical data, ensuring timely, high-quality deliverables for projects and submissions. You will be part of a programming team, handling medium to high-complexity work with minimal guidance. You collaborate with cross-functional members to meet project goals and continuously improve programming quality and efficiency. You will contribute to departmental innovation and uphold training and compliance standards, shaping robust analysis for clinical research.
Responsibilities- Designs and develops statistical programs for clinical research analysis and reporting
- Performs quality control and verification of programming outputs
- Maintains programming documentation
- Delivers medium to high complexity tasks with quality and timeliness
- Follows departmental processes and procedures
- Collaborates with statistical programming and cross-functional teams
- Reviews requirements and data to identify gaps and improve efficiency
- Contributes to departmental innovation and process improvement projects
- Experience as statistical programmer in a clinical research environment
- Strong statistical programming knowledge and ability to develop and verify code
- Ability to work within cross-functional teams and communicate effectively
- Attention to detail and commitment to high-quality deliverables
- Familiarity with GCP and clinical trial data handling
- Knowledge of SAS programming and statistics
- Collaborates effectively
- Detail-oriented
- Technologically savvy
- SAS Programming
- Statistical analysis
- Data modeling
Reference: WJ-747_30179048