Description
Purpose Statement:
Monitors progress of clinical studies at the site level to verify that the rights and well being of subjects are protected, that the reported study data are accurate, complete, and verifiable from source documents, and that the study is conducted in accordance with protocol, standard operating procedures, ISO/GCP and other applicable regulatory requirements. Provides support in start up, enrollment, follow up and closure of clinical trial activities.
Ready to Seal the Deal?
Submit your application today and take the next step in your career with Boston Scientific.
Apply for this Job