Sr. CRA 1 - Site Management (Clinical Research)

Location: Manchester, 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

• Conduct site selection, initiation, monitoring, and close-out visits in accordance with the study protocol, Good Clinical Practice, regulations, and sponsor requirements.
• Support subject recruitment plans and track recruitment, enrollment, regulatory submissions, approvals, CRF completion, and data query resolution.
• Train assigned sites on study protocols and maintain regular communication to manage expectations, issues, and project progress.
• Evaluate site practices, escalate quality issues, and verify that Trial Master File and Investigator Site File documentation is complete and compliant.
• Prepare monitoring visit reports, follow-up letters, action plans, and other required study documentation.
• Collaborate with study teams and, where applicable, support site financial management and invoice retrieval.

Requirements

• Bachelor’s degree in a scientific or healthcare discipline preferred.
• At least two years of on-site monitoring experience.
• Knowledge of clinical research regulations, Good Clinical Practice, and International Conference on Harmonization guidelines.
• Good command of written and spoken English, with strong communication, organizational, and problem-solving skills.
• Proficiency with Microsoft Word, Excel, PowerPoint, and laptop, iPhone, and iPad use where applicable.
• UK visa sponsorship is not available; existing UK work authorization is required.

Culture & Benefits

• Opportunity to contribute to the development and commercialization of medical treatments.
• Professional growth within hirify.global’s expanding UK Site Management team.
• Work with clinical research sites, sponsors, clients, and international study teams.