Clinical Trial Assistant

Responsibilities

• Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) teams with updating and maintaining clinical documents and systems, such as the Trial Master File (TMF).
• Prepare, handle, distribute, file, and archive clinical documentation and reports in accordance with standard operating procedures.
• Perform periodic reviews of study files to ensure completeness and compliance.
• Support the preparation, handling, and distribution of Clinical Trial Supplies and maintain accurate tracking information.
• Assist with the tracking and management of Case Report Forms (CRFs), queries, and clinical data flow.
• Serve as a central point of contact for designated project communications and correspondence.
• Accompany CRAs on site visits to assist with clinical monitoring duties upon completion of required training.

Requirements

• Bachelor's Degree.
• 3 years of administrative support experience (or an equivalent combination of education, training, and experience).
• Proficiency in Microsoft Word, Excel, and PowerPoint.
• Strong written and verbal communication skills with fluency in English.
• Excellent time management and organizational skills.
• Ability to establish and maintain effective working relationships with coworkers, managers, and clients.
• Awareness of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.

About the Company

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide.