Experienced Clinical Research Associate

Location: Reading, Berkshire, United Kingdom. Full UK right to work is required; the position is not eligible for visa sponsorship.

Company

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

What you will do

• Perform site selection, initiation, monitoring, and close-out visits for interventional clinical studies.
• Drive and track subject recruitment plans and manage study expectations with clinical sites.
• Deliver protocol and study training and maintain regular communication with assigned sites.
• Evaluate site quality, protocol conduct, and compliance with GCP, ICH, and applicable regulations.
• Track regulatory submissions, approvals, recruitment, enrollment, CRF completion, and data query resolution.
• Maintain TMF and ISF documentation, prepare monitoring reports, follow-up letters, and action plans, and collaborate with study teams.

Requirements

• At least 2 years of on-site monitoring experience in interventional studies.
• Degree in a scientific or healthcare discipline, or equivalent industry experience.
• Good knowledge of and ability to apply GCP, ICH, and applicable clinical research regulations.
• Ability to establish and maintain effective relationships with coworkers and clients.
• Full UK right to work required.
• Visa sponsorship is not available for this position.

Culture & Benefits

• Career development opportunities.
• Flexible working to support work-life balance and professional success.
• Well-being support covering physical, mental, and financial health.