Details:
- Compensation: $70 - $72/hour
- Benefits: Medical, Dental, Vision
- Employment Classification: FSP
- Status: On-Site
- Job ID: 21205
We are seeking an experienced Senior SAS Programmer contractor to support clinical programming activities for phase 2 studies. The ideal candidate will have strong technical expertise in SAS programming and CDISC standards, with particular emphasis on ADaM dataset validation. This role requires immediate contribution to ongoing clinical studies and regulatory submission preparations.
Key Responsibilities
Required Qualifications
Preferred Qualifications
Key Responsibilities
- Validate ADaM datasets based on raw data following study specifications, including consistency checks against SDTM and analysis results
- Create and validate Tables, Figures, and Listings (TFLs) per statistical analysis plans
- Ensure programming deliverables meet quality standards and regulatory compliance requirements
- Collaborate with biostatistics and data management teams on study deliverables
- Contribute to process improvement initiatives and maintain proper documentation and traceability
Required Qualifications
- Bachelor's or Master's degree in Statistics, Computer Science, or related field
- 5+ years of SAS programming experience in pharmaceutical/CRO setting
- Extensive hands-on experience with CDISC standards (SDTM/ADaM)
- Proven experience in ADaM validation activities
- Proficiency in Base SAS, SAS/STAT, and SAS Macros
- Strong understanding of clinical data structures and regulatory guidelines
Preferred Qualifications
- Experience with Pinnacle 21 Enterprise/Community
- Experience working in a contract capacity
- Familiarity with programming automation and efficiency improvement techniques