Senior Statistical Programmer-India

About the role

The Senior Statistical Programmer will lead single and/or multiple clinical trials and be responsible for the development, maintenance, and validation of annotated Case Report Forms (aCRFs) as well as of specifications and statistical programming of Standard Data Tabulation Model (SDTM) datasets, Analysis Data Model (ADaM) datasets (or derived datasets, as applicable), Tables, Listings, and Figures (TLFs), and submission packages required for various purposes including, but not limited to, Data…

What you'll do

• Act as a Lead Statistical Programmer on multiple single studies
• Review the statistical programming scope of work and budget at initiation of clinical trials and identify tasks that are out of scope
• Review and provide input into various DM documents (e.g., eCRF, edit checks, etc.), SAPs, and TLF Shells
• Use global SAS macros to increase efficiency of the statistical programming of SDTMs, ADaMs, derived datasets, and TFLs
• Act as Unblinded Primary or QC Statistical Programmer for randomization plans and lists, IDMCs, and IAs

What you need

• 5–9 yrs of experience
• SAS
• Clinical research
• SAP
• CRO
• Medication administration
• Communication
• Any graduate

Good to have

• VBA
• SOP writing