Clinical Research Associate (Oncology)

Location: Reading, Berkshire, United Kingdom; travel to clinical sites across the UK is required.

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 for oncology studies in accordance with contracted scope and Good Clinical Practice.
• Support site recruitment plans and track recruitment, enrollment, regulatory submissions, approvals, and study progress.
• Deliver protocol and study training to assigned sites and maintain regular communication to manage expectations and resolve issues.
• Evaluate site practices, protocol compliance, and data quality, escalating quality issues when required.
• Maintain study documentation, including visit reports, follow-up letters, Trial Master File records, and Investigator Site Files.
• Collaborate with study team members to support project execution and resolve data queries.

Requirements

• Experience independently conducting on-site monitoring for unblinded oncology studies.
• In-depth knowledge of Good Clinical Practice and International Conference on Harmonization guidelines.
• Degree in life sciences or equivalent industry experience.
• Flexibility to travel to clinical sites across the UK as required.
• This role is not eligible for visa sponsorship.

Culture & Benefits

• Full-time employment focused on clinical research and improving patient outcomes.
• Opportunities to build a career in life sciences and healthcare intelligence.
• Continuous learning through study protocols, site training, and project collaboration.