(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.