Candace Spruill

About Candace Spruill

Historical clinical research activities includes data collection and entry, regulatory document maintenance, quality assurance, development of SOP\'s and improving work processes during various trial phases while in connection with prominent CRO.

Experience

1. Clinical Trial Assistant

   IQVIA

   Oct 2019 — Present

   Responsible for assisting the clinical research teams in ensuring the most effective and efficient conduct of clinical research studies by providing administration and project tracking support.• Assist Clinical Team Lead (CTL) and Clinical Research Associates (CRAs) with accurately updating and maintaining clinical systems that track site compliance and performance within project timelines.• Assist the clinical team in the preparation, handling, distribution, filing, and archiving of clinical documentation and reports according to the scope of work and standard operating procedures. • Assist with periodic review of study files for accuracy and completeness.• Assist CTLs with preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.• Assist with the tracking and management of Case Report Forms (CRFs), queries and clinical data flow.• Act as a central contact for the clinical team for designated project communications, correspondence and associated documentation.• May perform assigned administrative tasks to support team members with clinical trial execution.