CRA I & CRA II

United Kingdom
December 18, 2025
Remote
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Job Description

Due to increased project demand, CRA I & CRA II professionals are urgently required to support a prestigious, world-leading pharmaceutical organisation on a fully dedicated single-sponsor FSP programme. This role offers the stability of a pharmaceutical environment combined with the structured career growth typically associated with a CRO model.

Key Responsibilities

  • Perform independent on-site and remote monitoring visits in line with ICH-GCP and UK regulatory requirements
  • Manage assigned clinical trial sites, ensuring protocol compliance and high data quality
  • Review clinical data, resolve queries, and ensure timely and accurate reporting
  • Maintain strong relationships with investigators and site staff to support trial delivery
  • Identify, escalate, and follow up on site issues, risks, and corrective actions
  • Ensure all trial documentation is complete, accurate, and inspection-ready

Requirements and How to Qualify
Candidates applying for the CRA I & CRA II role should meet the following criteria:

  • 6–18 months of independent on-site monitoring experience within the UK
  • Strong working knowledge of ICH-GCP guidelines and UK regulatory frameworks
  • Proven ability to manage sites proactively and work in a structured environment
  • Excellent organisational, communication, and time management skills
  • Valid full UK driving licence

What’s on Offer

  • Highly competitive salary package
  • Car allowance
  • Clear, structured career progression pathway
  • Long-term role stability within a single-sponsor programme
  • Opportunity to work on high-profile pharmaceutical projects

Engagement Model: 100% Single-Sponsor FSP

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