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Clinical Research Associate II

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Location:
United Kingdom , Reading

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Category:
Nursing

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Contract Type:
Employment contract

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Salary:

Not provided
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Job Description:

We are seeking a Clinical Research Associate to join ICON Commercialisation & Outcomes (ICO) — our Late Phase business. This is an exciting opportunity to work on post-marketing, real-world, and late phase studies, supporting evidence generation that demonstrates value, safety, and effectiveness in broader patient populations. As a CRA in our Late Phase team, you will play a critical role in ensuring high-quality delivery across a mix of interventional (IP) and medical device studies, contributing to successful outcomes that shape clinical and commercial strategy.

Job Responsibility:

  • Conduct on-site and remote monitoring visits across late phase studies, ensuring compliance with protocols, ICH-GCP, regulatory requirements, and applicable device regulations
  • Support execution of post-authorisation, observational, and interventional studies, ensuring high-quality data collection and real-world evidence generation
  • Evaluate site performance, identify risks, and implement solutions to ensure studies are delivered on time and to quality standards
  • Partner with project teams, medical, data management, and commercial stakeholders to ensure efficient study delivery and reporting
  • Provide guidance and support to site personnel and junior CRAs, maintaining consistency and best practice across both device and IP trials
  • Build strong relationships with investigators and site staff to drive engagement and successful study execution

Requirements:

  • Advanced degree in Life Sciences, Nursing, Pharmacy, or Medicine
  • Significant experience as a Clinical Research Associate, ideally within late phase / Phase IV / real-world studies
  • Experience across both investigational product (IP) and medical device trials is highly desirable
  • Strong understanding of ICH-GCP, regulatory requirements, and post-marketing study environments
  • Proven ability to manage multiple sites and competing priorities
  • Expertise in site monitoring, data integrity, and risk-based monitoring approaches
  • Proficiency in clinical systems (e.g., CTMS, EDC)
  • Willingness to travel across the UK (~6–8 days per month)
  • Excellent communication, stakeholder management, and influencing skills
What we offer:
  • Various annual leave entitlements
  • A range of health insurance offerings to suit you and your family’s needs
  • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead
  • Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being
  • Life assurance
  • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others

Additional Information:

Job Posted:
May 04, 2026

Employment Type:
Fulltime
Work Type:
On-site work
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