Position: Senior SAS Programmer
Location: Remote
Duration: 2 Years Contract to extend
Rate: Based on experience
A breakthrough pharmaceutical company is seeking a senior SAS programmer. The senior SAS programmer will collaborate closely with other programmers, biostatisticians, and clinical data managers. The senior SAS programmer will be accountable for leading collection, analysis, and reporting of clinical data for phase I-IV of clinical progress. The senior SAS programmer will be responsible for, but not limited to:
Responsibilities:
- Writes specifications for SDTM datasets, as well as ensuring the Study Data Tabulation Model Implementation Guide
- Implementing statistical analysis plans and the Analysis Data Model (ADaM) Implementation Guide, also composes specifications for analysis datasets
- Generates data entries, summary tables and graphs using SAS software
- Verifies data listings, summary tables and graphs, imports, and exports SAS data
- Supports data management group in executing data edit checks
- Upholds and applies work coherent with GCP, ICH, 21 CFR part 11, internal SOPs and training, and international regulatory requirements.
Qualifications:
- Experience and working knowledge utilizing SAS for statistical analysis
- Awareness of drug and clinical development process
- Outstanding attention to detail and scientific rigor
- Minimum of 5 years of experience as SAS programmer within pharmaceutical, biotechnology, medical device, and Clinical Research Organization (CRO)
- Experience with SDTM and ADaM industry data standards
- Bachelor's degree in statistics, computer science, or a relevant field
*W2 applicants only
Benefits:
- Remote Opportunity
- Health Benefits (Dental, Vision, Medical)
- Competitive Pay
- W2
