Job Title : Principal SAS Programmer (Clinical)
Location : Remote Work
Type : 6-12+ Months Contract
Salary : Market
Qualifications / Requirements / Skills :
- B.S., M.S., or Ph.D. degree in statistics, biostatistics, computer science or closely related field with a minimum of 7 years pharmaceutical / medical device / CRO related experience as a SAS programmer analyzing clinical trial data
- Excellent working knowledge of Base SAS (including macro language, Proc SQL, and ODS), SAS / GRAPH, and SAS / STAT
- Good working knowledge of CDISC SDTM and ADaM models
- Experience in integrating ISS / ISE data preferred
- Experience using other statistical packages (e.g., S-plus, R) a plus
- Knowledge of and ability to adhere to GCP principles and relevant regulatory requirements
- An aptitude for quantitative problem-solving with the capacity to troubleshoot and work independently
- Ability to follow guidelines and specifications on validation procedures and data transfer procedures
- Strong communication skills with the ability to interface at all levels; comfortable communicating workload to assist in managing priorities
- Flexible; ability to adapt to changing priorities and work independently with minimal supervision
- Experience running SAS in a Windows environment
Able to set realistic timelines for assigned tasks and follow through to completion