Clinical SAS SDTM
HCL America Inc. North Wales
HCL Technologies Limited
Key Responsibilities:- Create advanced SAS macros, templates, and utilities for efficient data processing
- Act as the primary programming point of contact for biostatisticians and study teams
- Perform peer review of code and documentation for accuracy and traceability
- Review CRF (Case Report Form) annotations and data specifications.
- Ensure compliance with CDISC standards (SDTM/ADaM) and FDA/ICH guidelines.
Skill Requirements:
- Extensive programming experience in a clinical trial environment (CRO/Pharma).
- Expertise in SAS/BASE, SAS/STAT, and SAS/MACRO.
- In-depth knowledge of CDISC standards and regulatory submission requirements.
- Must have 5-7 yrs of exp in clinical domain
- Strong knowledge of SDTM.
Disability SolutionsSpring House
the diversity and dignity of our employees and recognize their merit.
Job Function: Discovery & Pre-Clinical/Clinical Development
Job Sub Function: Translational Discovery & Development Biomarkers
Job Category: People Leader
All Job Posting Locations: San Diego...
Disability SolutionsSpring House
the diversity and dignity of our employees and recognize their merit.
Job Function: Discovery & Pre-Clinical/Clinical Development
Job Sub Function: Translational Discovery & Development Biomarkers
Job Category: Scientific/Technology
All Job Posting Locations...
Disability SolutionsHorsham, 7 mi from North Wales
the diversity and dignity of our employees and recognize their merit.
Job Function: Quality
Job Sub Function: Clinical Quality
Job Category: Professional
All Job Posting Locations: Horsham, Pennsylvania, United States of America, Raritan, New Jersey...