About this role

Completes and may lead programming trial activities of low to medium complexity
Accountable for the design and development of programs in support of clinical research analysis
Performs verification of programming and reporting activities
Supports submission activities including CDISC compliant data packages
Follows departmental processes and procedures
Collaborates effectively with team and cross-functional members
Ensures compliance with required training and business processes

Bachelor’s degree or higher in computer science, data science/data engineering, mathematics, public health, or relevant scientific field
Approx. 2+ years of relevant programming experience
Basic knowledge of regulatory guidelines (e.g. ICH-GCP)
Excellent written and verbal communications skills
Knowledge of data structures and programming languages such as SAS, R, Python
Basic knowledge of processes, methods, and concepts relevant to programming

Experienced Statistical Programmer

Key skills