The programmer will be responsible for all programming aspects (analysis datasets, pooled datasets, listings and tables) of individual clinical trials as needed. Supervise CROs as required and ensure timely deliverables with highest quality.
Lead the programming activities for a trial or publication activities.
Maintain efficient interfaces with internal and external customers with support of CDS management, Program Programmer/Statistician and CPOs as needed.
Develop resource plans as required with support of the Program Programmer.
Graduate with 5-7 of experience in a programming role preferably supporting clinical trials/ or in the pharmaceutical industry.
Key skills :
1.Working on Analysis with SAS on the data, related to Clinical trials (Safety or Ephicacy data).
2.Should be working on Tables, listings and graphs.
3.Generating programme related MACROS.