Clinical SAS Programmer/Biostatistician/Statistical Programmer

- Good Clinical Domain knowledge understanding clinical phases and Work expr must be in clinical domain with min 2 projects (Phase I-IV).

- Create Data transfer specification by referring the eCRF, Annotation of eCRF, knowledge on Protocol.

- Create SAS datasets of clinical data from raw data; create status and efficacy datasets; create project specific macros and formats; load client data from other platforms; prepare data to be sent to clients.

- Create listings and Custom reports as per customer requirement.

- Knowledge on Vendor Import programmer

- Strong Technical knowledge on SAS programming, CDISC SDTM standards, Semi SDTM (Sponsor based standards).

- SAS /BASE, SAS/Advance SAS, SAS/ Macros, SAS/SQL & SAS/SAS Grid knowledge is required.

- Data listings, in accordance with approved statistical analysis plan and shell displays for clinical research studies.

- Code is to be written using Base SAS programs, SAS procedures, or standardized macros. Perform data checks

- as needed to understand structure and content of data.

- Coordinate the different project stake holder on project deliverables.

- Create and maintain Standard QC documentation and maintain the accuracy.

- Good Communication skill