These are the main tasks:
-Prepare high quality SAS programs to generate tables, listings, and
graphs for clinical trial data.
-Validate SAS programs according to Client's SOPs.
-Contribute to the creation of programming specifications.
-Define and test the mapping of clinical trial data into the Generic
Data Model.
The candidate should have experience with the first three bullets plus
good communication. They are looking for people with at least 7 years
+ experience with SAS within the Pharma industry.
We are looking to find programmers who have project lead experience.
Client wants someone who can lead rather than just a program,
preferably 2 years project management.
Please send all resumes and inquiries please email me at
Jtere...@designstrategy.com