Dartford

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Job Description

(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.

Required Knowledge, Skills, and Abilities