Clinical Trials Support Specialist – On-Site (Maidenhead)

IQVIA LLC

Thatcham

On-site

GBP 26,000 - 35,000

Full time

14 days+

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Job summary

IQVIA in Maidenhead, Berkshire, is seeking a Clinical Trials Assistant to support the cFSP sponsor-dedicated team. The role involves maintaining trial master files, preparing and filing documents, and assisting with trial supply logistics.

The ideal candidate has prior clinical trials support experience, knowledge of GCP/ICH, a life sciences degree, and strong English communication. Proficiency with Word, Excel, and PowerPoint, plus excellent organization and collaboration skills, are essential.

Qualifications

Previous clinical trials support experience.
Knowledge of GCP and ICH regulatory requirements.
Degree in life sciences or related field.
Proficiency in MS Word, Excel and PowerPoint.
Excellent written and verbal communication in English.
Strong time management, organization and collaboration skills.

Responsibilities

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