The Senior Statistical Programmer is an independent statistical programmer analyst supporting the clinical reporting production programming and verification for client regulatory submissions and publications. This is a full-time (40 hrs/week), fully remote position.
Responsibities:
-Independently develop SAS or other programs and specifications for use in study or other analyses
-Work with clinial data management staff and biostatisticians to coordinate and scedule data transfers and delivery of required outputs
-Oversee the development of datasets in SDTM format by CROs
-Responsible for programming QC oversight of CRO deliverables such as analysis datasets and tables, listings, and figures
-Adhere to FDA regulations
-Produce study datasets and programs that will help meet CDISC standards
Requirements:
-At least 6 years industry experience with SAS programming in pharmaceutical industry
-Proficiency in SAS
-Knowledgeable of CDISC, SDTM, and ADaM standards
-Previous experience with oncology preferred
-Ability to work in Unix/Linux environment
