East London Postnatal Doula & Newborn Care Expert
Core
Senior statistical programmer developing clinical trial data standards, datasets, and analysis programs for pharmaceutical clients.
Role type
Senior IC statistical programmer (SAS/R)
Builds
CDISC-compliant datasets, statistical listings, tables, and regulatory submission packages
Domain
Biopharmaceutical clinical development and regulatory affairs
Required skills
SAS programming, CDISC standards (SDTM, ADaM, Define.xml), clinical trial methodologies, FDA/ICH regulations, data validation, regulatory submissions
Preferred skills
R programming, Python, pharmacokinetic data analysis, neuroscience domain knowledge
Technologies
SAS, R, Unix/Linux, git, Shiny, Markdown
Responsibilities
Generate SDTM, ADaM specifications and datasets; Develop SAS programs for complex listings and tables; Validate and maintain statistical programming tools; Oversee CRO programming deliverables; Support clinical study reports and regulatory submissions; Collaborate with cross-functional teams on project timelines
Seniority
Senior, hands-on IC
