Clinical SAS Programmer - Pharma

Primary Purpose

The Clinical SAS Programmer is responsible for assisting the development of statistical programs and reports to analyze clinical trials in accordance to the project requirements

Responsibilities:

 - Assists in preparation of clinical programming activities such as data cleaning, extraction and integration programs, web reporting programs, integrity reports, analysis datasets, CDISC SDTM and ADaM data mappings, CSR tables, listings and figures (TLF), ad hoc reports etc. 

- Assisting documentation of SAP, mock shells, randomization plan, analysis data specification and other documents within capacity of clinical programming. 

- Provides accurate, effective and timely communication of clinical study and defects to senior members of the team. 

- Understand the requirement of specific validation process for the project and help to document them.

Experience:

- Requires a Master's Degree/Bachelor's Degree in Mathematics, Statistics, Engineering, Computer Science/Applications, Pharmacy, or any other similar type of qualification

- At least 2-4 years of SAS experience as a Clinical SAS programmer in Pharmaceutical/CRO

- Good knowledge of programming languages (SAS Macros, SQL etc.) with understanding of databases.

- Good analytical skills with the ability to process scientific and medical data.

- Knowledge in development, documentation, and testing of analysis data and programming code to meet regulatory and company standards.

- Understanding of GCP principles and other regulatory standards in Clinical Research.

- Good organizational and communication (written and oral) skills, ability to manage multiple tasks, ability to work with minimum supervision, as well as in a team environment and a desire to improve skills