Strong experience working with at least two system used within the Clinical Trial process (e.g.
SAS, CDMS, EDC (Inform, RAVE, DataLabs, Medrio, Veeva), CTMS, Medical Safety Reporting)
is desirable. Build Certified in at least one system, if available
Strong experience in clinical research industry or similar field is required
Knowledge of Software Development Life Cycle (SDLC) methodologies. Knowledge of GCP,
21CFRPart11 and other relevant ICH/regulatory guidelines
Team and Project leadership experience required.
Education:
Bachelor s degree (or equivalent) in a relevant science discipline is preferred or equivalent work
experience.
Keyskills: clinical data management programming biomedical root cause global teams clinical data
As part of Parexel Consulting, you will create and maximize value for clients throughout the product lifecycle. You will be a strategic guide in getting products to market faster, smarter – and keeping them there –your scientific, technical, regulatory, and/or commercial expertise will...