Clinical Research Associate – South West England

About the role

Join IQVIA on its mission to accelerate innovation for a healthier world. The UK cFSP (sponsor‑dedicated) team is expanding and is looking for experienced Clinical Research Associates to support studies in South West England.

Key responsibilities

• Perform site monitoring visits (selection, initiation, monitoring and close‑out) in line with GCP and ICH guidelines.
• Collaborate with sites to drive subject recruitment plans and track enrollment progress.
• Provide protocol training to sites and maintain regular communication to manage expectations.
• Assess site practices for quality and regulatory compliance, escalating issues when needed.
• Track regulatory submissions, CRF completion, data queries and study progress throughout the trial lifecycle.

Required profile

• Minimum 2 years of independent on‑site monitoring experience on interventional studies.
• Experience across study start‑up, enrolment, maintenance and close‑out phases.
• Degree in a scientific discipline or equivalent healthcare industry experience.
• Full UK right to work; visa sponsorship is not available.

Required skills

• Digital literacy with confidence using AI tools in a professional setting.
• Good Clinical Practice (GCP) knowledge.
• International Conference on Harmonisation (ICH) guideline expertise.

What we offer

• Career development opportunities through an internal talent marketplace and mentorship programmes.
• Flexible working arrangements to support work‑life balance.
• Well‑being support covering physical, mental and financial health.
• Recognition as a Glassdoor “Best Place to Work” and Fortune “World’s Most Admired Companies”.