Completes and may lead programming trial activities of low to medium complexity
Designs and develops programs in support of clinical research analysis and reporting
Performs verification of programming and reporting activities
Collaborates effectively with team and cross-functional members

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

Experienced Clinical Programmer

Key skills