Clinical Trial Assistant I - Redwood City
1 week ago
Job summary
Assist with the distribution of key study documents such as investigator brochures protocols informed consent forms interim safety reports and site educational and reference material Assist with formatting and production of site facing materials Maintain and perform routine reviews of the Trial Master File Assist project team with investigator recruitment by obtaining confidentiality agreements forwarding study synopsis to sites and distribution of feasibility questionnaires Facilitate collection of regulatory documents for initial internal IP and regulatory release Coordinate collection tracking and maintenance of updated site regulatory documentation Track ship as needed study supplies provided by Corcept and study specific vendors Set up maintain study tracking tools with oversight of manager Develop working knowledge company standard operating procedures SOPs FDA regulations related clinical studies Provide general administrative support Clinical Operations Department Other duties assigned manager
Job description
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