Convert study design and specifications into programs to support clinical trials. Validate S A S programs written by others. Assists Management in maintaining SOPS and work instructions relevant to S A S programming. Follow regulatory requirements and guidelines for the development, usage, and maintenance of programs to support regulatory submissions. Disseminate the programming activities for a clinical trial to a junior level. Write and maintain documentation to describe program development, logic, coding, testing, and updating.
https://www.indeed.com/viewjob?t=principal+sas+programmer&jk=00fd2429c9147e8d&_ga=2.199772206.1883655580.1560177893-1429968906.1557248850
No comments:
Post a Comment