Corcept Therapeutics is hiring a
Clinical Trial Assistant I

Summary

Join a dynamic team at Corcept as Clinical Trial Assistant and contribute to advancing the possibilities of cortisol modulation in treating serious diseases.

Requirements

• BA/BS or equivalent work experience
• 0-5 years’ experience in pharma related industry

Responsibilities

• Assist with formatting/production and distribution of key study documents such as investigator brochures, protocols, informed consent forms, interim safety reports, and site educational and reference material
• Assist project team with study specific documentation including filing to the Clinical Trial Management System and Trial Master File
• Maintain Trial Master File by setting up and using tracking tools
• Assist with investigator recruitment by making initial site contact, obtaining confidentiality agreements, forwarding study synopsis to sites and administering feasibility questionnaires
• Assist project team with gathering agenda topics, preparing agenda, scheduling meetings, attend and generate project meeting minutes
• Facilitate submission of regulatory documents to/for a central institutional review board (IRB) and coordinate collection, tracking, and maintenance of updated site regulatory documentation
• Participate in organizing investigator meetings including venue investigation, selection, invitations, agenda and materials distribution
• Track clinical supply inventory at sites and manage the site drug re-supply process
• Set-up and maintain tracking system with oversight of manager
• Develop working knowledge of company standard operating procedures (SOPs) and FDA regulations related to clinical studies
• Provide general administrative support to the Clinical Operations Department

Benefits

$83,100 - $97,800 pay range