Statistical Programmer role developing clinical trial analysis programs for Johnson & Johnson. Collaborating with cross-functional teams on clinical research projects while using programming languages like SAS and R.
Responsibilities
Completes and may lead programming trial activities of low to medium complexity and/or criticality, with high quality and timeliness of deliverables
Accountable for the design and development of programs in support of clinical research analysis and reporting
Performs appropriate level of verification of programming and reporting activities
Reviews and provides input for project requirements and documentation
Supports submission activities including but not limited to creation, verification, and delivery of CDISC compliant and/or non-standard data packages and reviewer’s guides
Follows departmental processes and procedures, ensures use of latest standards and deployment of current technologies
May contribute to departmental innovation and process improvement projects
Collaborates effectively with team and cross-functional members
Ensures continued compliance with required company and departmental training, time reporting and other business/operational processes as required for position
Requirements
Bachelor’s degree or higher and/or equivalent in computer science, data science/data engineering, mathematics, public health, or another relevant scientific field (or equivalent theoretical/technical depth)
2+ years of relevant programming experience, preferably in Pharmaceutical, CRO or Biotech industry or related field or industry
Basic knowledge of processes, methods, and concepts relevant to programming
Basic knowledge of regulatory guidelines (e.g. ICH-GCP) and relevant clinical R&D concepts
Knowledge of data structures and relevant programming languages for data manipulation/statistical analysis and reporting (SAS and R required)
Excellent written and verbal communications skills
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