Candidate will be hands on to work on IP hardware and client/server/database applications. Responsibilities include develop tools/software, manual test, automation test, setup/maintain test environment, and create test cases/matrix/report.
Should have a diverse knowledge of GCP regulations and other regulatory guidance documentation as it applies to appropriate procedures to validate computerized systems used to capture and analyze data for clinical research .
Responsible for developing automated test scripts. Dedicated to QA efforts utilizing a diverse set of tools / technologies working closely with members of the development team to ensure all requirements and expectations are met.