SR CRA I

Location: Manchester, United Kingdom

Company

IQVIA 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 interventional clinical studies.
• Support subject recruitment plans and track recruitment, enrollment, regulatory submissions, and approvals.
• Deliver protocol and study training to assigned sites and manage ongoing communication, expectations, and issues.
• Evaluate site quality, protocol compliance, and adherence to GCP, ICH, and applicable regulations.
• Maintain monitoring documentation, visit reports, follow-up letters, site files, and Trial Master File records.
• Collaborate with study team members to support project execution and resolve data queries.

Requirements

• 3–5 years of on-site monitoring experience with interventional studies.
• Degree in a scientific or healthcare discipline, or equivalent industry experience.
• Strong knowledge of Good Clinical Practice, International Conference on Harmonization guidelines, and clinical research regulations.
• Ability to establish and maintain effective working relationships with coworkers and clients.
• This position is not eligible for visa sponsorship.

Culture & Benefits

• Flexible working arrangements supporting work–life balance and professional success.
• Career development opportunities and learning support.
• Well-being support for physical, mental, and financial health.