Clinical Trials Assistant II

Location: Reading, Berkshire, United Kingdom

Company

hirify.global provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

• Maintain and update Trial Master Files and other study documentation.
• Prepare, file, track, and archive clinical trial documents.
• Review study files for completeness and regulatory compliance.
• Coordinate clinical trial supplies and tracking records.
• Assist with CRF tracking, study queries, and data workflows.
• Serve as a key contact for project communications and documentation.

Requirements

• Previous administrative, coordination, or healthcare-related experience.
• Proficiency in Microsoft Word, Excel, and PowerPoint.
• Strong organization skills and attention to detail.
• Ability to manage multiple priorities and meet deadlines.
• Effective communication and collaborative working skills.
• Science degree preferred.

Culture & Benefits

• Full-time role supporting clinical research and healthcare innovation.
• Opportunity to work closely with Clinical Research Associates and Regulatory teams.
• Exposure to the clinical research process and study coordination.
• UK visa sponsorship is not available for this role.