Clinical Trials Assistant I (Clinical Research)

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.
• Support project communications and documentation as a key contact.

Requirements

• Passion for clinical research and healthcare.
• A science degree is preferred.
• Previous administrative, coordination, or healthcare-related experience, or an equivalent combination of education, training, and experience.
• Proficiency in Microsoft Word, Excel, and PowerPoint.
• Strong organizational skills, attention to detail, and the ability to manage multiple priorities and meet deadlines.
• Effective communication and collaborative working skills.

Culture & Benefits

• Full-time employment supporting clinical research and healthcare innovation.
• Opportunity to gain exposure to the clinical research process while working with Clinical Research Associates and Regulatory teams.
• This role is not eligible for UK visa sponsorship.