Clinical Trial Assistant At IQVIA
New Cairo, Egypt
Responsibilities:
Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) with accurately updating and maintaining clinical systems that track site compliance and performance within project timelines.
Collaborate on 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 and completeness.
Collaborate on the preparation, handling and distribution of Clinical Trial Supplies and maintenance of tracking information.
Coordinate 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.
Perform assigned administrative tasks to support team members with clinical trial execution.
Requirements:
Computer skills including proficiency in use of Microsoft Word, Excel and PowerPoint
Effective written and verbal communication skills
Effective time management and organizational skills
Ability to establish and maintain effective working relationships with coworkers, managers and clients
Good command of English language.
Basic knowledge of applicable clinical research regulatory requirements; i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines is preferred
Previous experience within a clinical trials environment is preferred.