Senior Clinical Research Associate

(SCRA) – UK (6–8 Site Visits/Month) – Global CRO

My client is a leading global Contract Research Organization (CRO), trusted by top pharmaceutical and biotech companies worldwide to deliver high-quality clinical research solutions. They are committed to advancing human health through innovation, collaboration, and scientific excellence.

The Opportunity

On behalf of my client, I am seeking an experienced Senior Clinical Research Associate (SCRA) to join their UK team. This position offers a balanced workload of 6–8 site visits per month, giving candidates the chance to work on impactful global studies while maintaining a sustainable travel schedule.

Key Responsibilities

• Conduct routine on-site monitoring visits in line with ICH-GCP, UK regulations, and sponsor SOPs.
• Develop and maintain strong site relationships to ensure high standards of performance and compliance.
• Perform source data verification (SDV), CRF review, and essential document checks.
• Identify and resolve site or protocol-related issues, escalating where required.
• Act as a resource and mentor for junior CRAs as needed.

Candidate Profile

• Minimum of 18–24 months’ independent monitoring experience as a CRA.
• Strong knowledge of ICH-GCP guidelines and UK regulatory environment.
• Multi-therapeutic area experience advantageous.
• Excellent communication, organizational, and problem-solving skills.
• Life sciences degree (or equivalent).
• Willingness to travel across the UK (6–8 site visits per month).

What’s on Offer

• Competitive salary and comprehensive benefits package.
• Flexible home-based working.
• Career progression opportunities within a global CRO.
• Supportive, collaborative working environment.