Clinical Trial Documentation & Compliance Assistant

IQVIA; Manchester; On-site; GBP 21,000 - 30,000; Full time

Benefits offered by this job

Autonomy

Global exposure

Team environment

Career development

Job summary

IQVIA's Medicines Evaluation Unit (MEU) in a hospital-based research facility is seeking an organised Clinical Trial Assistant. You will support CRAs and the RSU team by maintaining Trial Master File records, handling clinical documents, and coordinating trial supplies and data flow.

This office-based role offers exposure to multiple therapeutic areas and a collaborative team environment. Responsibilities include preparing and filing documentation, ensuring SOP compliance, and acting as a

Qualifications

• High School Diploma or equivalent.
• 2-3 years of relevant experience.
• Must have commercial experience.
• Computer skills including working knowledge of Microsoft Word, Excel and PowerPoint.
• Written and verbal communication skills including good command of English language.
• Clinical research experience preferred.

Responsibilities

• Assist CRAs and RSU with updating and maintaining TMF and other clinical documents.
• Prepare, handle, file and archive clinical documentation and reports per SOPs.
• Assist with Clinical Trial Supplies handling and distribution; track CRFs and data flow.
• Serve as central contact for project communications and documentation for designated projects.
• Perform daily administrative tasks to ensure complete and accurate Trial Master File delivery.

Skills

Microsoft Word

Microsoft Excel

PowerPoint

Written and verbal communication

English language proficiency

Education

High School Diploma or equivalent

Tools

MS Office suite

Job description

IQVIA's Medicines Evaluation Unit (MEU) in a hospital-based research facility is seeking an organised Clinical Trial Assistant. You will support CRAs and the RSU team by maintaining Trial Master File records, handling clinical documents, and coordinating trial supplies and data flow.

This office-based role offers exposure to multiple therapeutic areas and a collaborative team environment. Responsibilities include preparing and filing documentation, ensuring SOP compliance, and acting as a