- 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
- Strong hands-on experience in SAS Programming & SDTM
- Knowledge of CDISC standards and clinical trials
- Experience in SDTM mapping and validation