Clinical Trials Assistant

As a Clinical Trials Assistant, you’ll play a vital role in supporting Clinical Research Associates (CRAs) and Regulatory & Start-Up (RSU) teams. Your contributions will ensure the accuracy, completeness, and compliance of essential clinical documentation, helping to maintain a high-quality Trial Master File and streamline study operations.

Key Responsibilities:

• Maintain and update clinical systems and documentation, including the Trial Master File.
• Support the preparation, distribution, filing, and archiving of clinical documents and reports.
• Conduct periodic reviews of study files to ensure completeness and compliance.
• Assist with clinical trial supply logistics and tracking.
• Manage Case Report Forms (CRFs), queries, and clinical data flow.
• Serve as a central point of contact for project communications and documentation.

What We’re Looking For:

• Degree in life sciences or equivalent industry experience.
• Familiarity with Good Clinical Practice (GCP) and ICH guidelines.
• Proficiency in Microsoft Word, Excel, and PowerPoint.
• Strong written and verbal communication skills in English.
• Excellent time management, organization, and collaboration skills.

Please note: This role is not eligible for UK visa sponsorship.

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. Learn more at https://jobs.iqvia.com