We are looking for a full time Clinical Trials Assistant to join our research site based in Pasadena, Ca area. The ideal candidate will have 2+ years' experience reviewing clinical regulatory documentation, trial master file (TMF) and EKG.

Description:
Accurately updated and maintain clinical system within project timelines
Taking patients vitals, EKG
Prepare, handle, distribute, file and archive clinical documentation and reports
Review of study files periodically for accuracy and completeness
Prepare, handle and distribute of Clinical Trial Supplies and maintenance of tracking information
Track and manage Case report Forms (CRFs), queries and clinical data flow
May act as a central contact for the clinical team for designated project communications, correspondence and associated documentation
Perform administrative tasks to support team members with clinical trial execution as needed

Requirements:
2+ years' experience reviewing clinical regulatory documentation and trial master file (TMF)
Must possess a general knowledge of applicable clinical research regulatory requirements including GCP and ICH guidelines
Must have strong critical thinking skills
Effective time management and organizational skills
Strong written and verbal communication skills