Sr SAS Programmer - Clinical Trials

As a Sr. SAS Programmer you need to understand Protocol, Statistical Analysis Plan, and CRF's and should have sound knowledge of all Phases (I-IV) of the Clinical Trials.

- Good Experience to Create summary tables, listings and graphs as per the Statistical Analysis Plan.

- Ability to write the specifications for the SDTMs, VAD and TLFs

- Perform validation of SAS programs to verify the final outputs.

If interested, please feel free to speak to Pallavi Deva at 09873412504