A company is looking for a Senior Statistical Programmer responsible for providing statistical programming services for assigned clinical trials.
Key Responsibilities
Act as the lead programmer for complex clinical trials and coordinate activities for support programmers
Design, develop, document, and validate tools and macros to enhance quality and efficiency
Train and mentor team members while participating in business development and SOP development
Required Qualifications
Degree in Statistics, Computer Science, or a closely related field; work experience may substitute for degree
Minimum of 6 years of direct SAS programming experience in pharmaceutical development or CRO environment
Good knowledge of medical terminology and clinical trial analysis
Familiarity with relevant industry data standards such as CDISC SDTM and ADaM
Senior Programmer • Kalamazoo, Michigan, United States