Description
The Clinical Programmer (SDTM) will create, validate, annotate, and quality-control SDTM datasets from raw clinical trial data, develop Define.xml and related regulatory documents, and support data submission packages. The role requires a bachelor’s degree in a relevant quantitative or life sciences field, 6 months to 2 years of SDTM programming experience, SAS and R proficiency, knowledge of CDISC standards, and familiarity with clinical trial protocols and adverse-event reporting. The employer offers flexible working options and other employee benefits.
