Responsibilities
Develop SDTM datasets and mapping specifications.
Transform clinical data into SDTM/ADaM deliverables.
Perform Define.xml generation and compliance validation.
Develop SAS macros, utilities, and automation programs.
Review programming deliverables and support study execution.
Collaborate with clients and contribute to project delivery.
Mandatory Requirements
Pharma/Clinical Research experience mandatory
Solid hands-on experience in SAS Programming & SDTM
Knowledge of CDISC standards and clinical trials
Experience in SDTM mapping and validation