We have a current opportunity for a Senior Statistical Programmer. My client is a highly renowned biotech company focusing within oncology and immuno-oncology cell therapies. This position is fully remote and begins on an initial 12 month contract with opportunity for extension or conversion.
Responsibilities:
-Independently develop SAS or other programs and specifications for use in study or other analyses
-Work with clinical data management staff and biostatisticians to coordinate and schedule data transfers
-Oversee the development of 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 regarding training records, guidelines, and SOPs
-Produce study dataset and programs that will help meet CDISC standards
-Meet timelines on a regular basis
Requirements:
-At least 6 years experience in statistical programming with clinical data and SAS
-Proficiency in SAS
-Knowledgeable of CDISC, SDTM, and ADaM standards
-Previous experience with oncology preferred
