Clinical Data Integration Specialist

Senior Biostatistical Programmer

We are seeking a detail-oriented Senior Biostatistical Programmer to support clinical trial data standardization, analysis, and regulatory submissions.

- Transform raw clinical trial data into CDISC-compliant SDTM and ADaM datasets;

- Develop, validate, and maintain Tables, Listings, and Figures (TLFs) for clinical study reports and regulatory submissions;

- Write efficient SAS programs for data cleaning, derivations, and reporting;

- Support programming QC and peer reviews to ensure accuracy traceability;

The ideal candidate will have strong expertise in CDISC standards (SDTM & ADaM), SAS programming,, TLFs generation experience. The position requires knowledge of TLFS creation process quality control submission processes. Basic Python or R scripting skills is an advantage.

Strong candidates should demonstrate attention documentation practices experience supporting audits inspections reproducible code documentation required preferred hands-on experience generating tables figures TLFs TDMPADAM datasets