Tasks: Responsible for developing, reviewing, finalizing, and maintaining clinical trial documents such as informed consent forms. Applies knowledge of GCP Guidelines, regulatory requirements, regulatory framework of privacy standards a...
Tasks: Responsible for developing, reviewing, finalizing, and maintaining clinical trial documents such as informed consent forms. Applies knowledge of GCP Guidelines, regulatory requirements, regulatory framework of privacy standards a...
this may have been adequate... Clinical Team Lead - Argentina Fortrea - Organic Trial Preparation, Conduct and Closeout:1...