California Licensed Clinical Trial Specialist

Job Summary

Providing logistical support for clinical trials, the remote California Licensed Clinical Trial Specialist will coordinate site start-up through close-out activities, manage vendor contracts, and maintain study documentation on a contract basis.

Key responsibilities

• Support the development, review, and maintenance of study documents, including site instructions and informed consent forms
• Set up and maintain trackers, tools, dashboards, and reports to monitor study metrics and support trial operations
• Oversee assigned vendor contracts, including invoicing and purchase order monitoring, with study lead oversight

Required qualifications

• Bachelor's degree or equivalent experience
• At least 2 years of direct work experience in Clinical Research
• Understanding of study phases and their application to Clinical Development
• Ability to manage multiple tasks and deadlines while identifying issues and taking appropriate action
• Experience with electronic Trial Master File systems