The Clinical Trials Assistant will play a vital role in supporting Local Trial Managers and Clinical Research Associates.

Key deliverables include tracking progress of the clinical trial, managing study data, budget, investigational products, mailings and correspondence and other relevant tasks in support of the Local Trial Managers and Clinical Research Associates.

Candidates must be able to commute to sponsor site for on site work in Buckinghamshire for hybrid working. We are seeking candidates with previous CTA experience to hit the ground running.

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.
Previous CTA 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

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Clinical Trials Assistant II