Senior CRA


London
Permanent
EUR60000 - EUR65000
Research and Development
PR/581261_1772015494
Senior CRA

Senior Clinical Research Associate (Biotech)

Location: Surrey (Hybrid: 2 days onsite / 3 days remote)
Contract: Permanent, full-time
Travel: Some travel required
Eligibility: Must live within 1.5 hours of Surrey

We´re recruiting a Senior Clinical Research Associate to drive site operations across both clinical trials and commercial distribution for an innovative therapy. You'll own feasibility, start-up, monitoring, and close-out, ensuring patient safety, data quality, and inspection readiness.

What you'll do

Clinical operations & site management

  • Lead feasibility and site evaluations; set up new sites end-to-end
  • Train, initiate, monitor, and close studies and commercial sites (incl. SCENESSE®)
  • Track study status, timelines, and quality; prepare high-quality visit reports
  • Manage site payment processes and reconciliation

Compliance, safety & quality

  • Conduct remote and onsite visits to ICH‑GCP, GxP, local/global regs, and SOPs
  • Safeguard subject rights, data integrity, and audit readiness
  • Oversee essential documents per ICH‑GCP/GVP; monitor PV and safety reporting
  • Support inspections/audits and CAPA follow‑up

Documentation & scientific contribution

  • Contribute to informed consents, monitoring plans, study manuals, protocols
  • Support CSR inputs, literature reviews, and publication activities
  • Maintain robust in‑house document quality management

Stakeholder engagement & improvement

  • Build strong site relationships; manage issues and escalate when needed
  • Participate in investigator meetings and represent at conferences
  • Train junior team members; identify and drive process improvements

What you bring

  • 5+ years as a CRA with hands‑on site monitoring and trial management
  • Strong working knowledge of ICH‑GCP, GxP, and GVP
  • Degree in Biological Sciences, Nursing, Pharmacy, or related field (postgrad a plus)
  • Excellent documentation, communication, and stakeholder management
  • Organized, proactive, detail‑driven, and comfortable with hybrid working
  • Able to travel as required and based within 1.5 hours of Surrey
  • Must have Right to Work in the UK

Why join

  • High-impact role at the intersection of science and delivery
  • Collaborate with experts and see real-world patient benefits
  • Fast-paced environment with meaningful ownership and growth

Interested? Apply now!

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