> Markdown version of [/jobs/ext/4704964-sdtm-technical-lead-sdtm-clinical-sas-python](https://www.wearedevelopers.com/jobs/ext/4704964-sdtm-technical-lead-sdtm-clinical-sas-python). Every page supports `.md` or `Accept: text/markdown`. Links point to the HTML versions so they work for humans too. Agent guide: [/agents.md](https://www.wearedevelopers.com/agents.md). --- # SDTM Technical lead SDTM -Clinical SAS Python - **Company:** Shrive Technologies Llc - **Location:** North Wales, PA, United States - **Experience:** Expert - **Salary:** $124,800 - $135,200 - **Contract:** Permanent contract - **Skills:** Clinical Data Repository, Computer Programming, Python (Programming Language), SAS (Software), SAS/Base, SAS/STAT, Data Processing, Scripting - **Published:** November 13, 2026 - **Apply:** https://www.careerbuilder.com/job-details/sdtm-technical-lead-sdtm-clinical-sas-python-north-wales-pa--d7d5ba47-1d20-42e9-918f-4a35593abdb9 ## About the Role Technical Leadership, Python Programming/Scripting Language, Statistical Analysis System (SAS), Python Programming/Scripting Language, Clinical Data Interchange Standards Consortium (CDISC), Clinical Trial, Data Processing, Maintain Compliance, Traceability, Regulatory Submissions, Mandatory skills- SDTM, Clinical SAS, Python Job Description- Looking for SDTM experts having in-depth knowledge of sas programming(macro's) 1.Must have 6-8 yrs of exp in clinical domain 2.Strong knowledge of SDTM 3.Create advanced SAS macros, templates, and utilities for efficient data processing 4.Act as the primary programming point of contact for biostatisticians and study teams 5.Perform peer review of code and documentation for accuracy and traceability 6.Review CRF (Case Report Form) annotations and data specifications. 7.Ensure compliance with CDISC standards (SDTM/ADaM) and FDA/ICH guidelines Skill: 1.Extensive programming experience in a clinical trial environment (CRO/Pharma). 2.Expertise in SAS/BASE, SAS/STAT, and SAS/MACRO. 3.In-depth knowledge of CDISC standards and regulatory submission requirements.