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

Bachelor’s degree or higher in computer science, data science/data engineering, mathematics, public health, or a relevant field
Approx. 2+ years of relevant programming experience, preferably in Pharmaceutical, CRO or Biotech industry
Basic knowledge of regulatory guidelines (e.g. ICH-GCP)
Experience working in a team environment
Excellent written and verbal communications skills
Knowledge of data structures and relevant programming languages for data manipulation/statistical analysis and reporting (SAS, R, Python, etc.)

Experienced Statistical Programmer

Key skills