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Senior CRA

ICON · Reading, UK

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Clinical OperationsFull-timeCompany career page

RoleLantern re-checked this role's application link recently and it was active — the employer has not confirmed it directly.

Role summary

Senior Clinical Research Associate position at ICON overseeing clinical trial monitoring and site management in a sponsor-dedicated model. Lead technical monitoring activities, conduct site visits, and provide guidance to ensure protocol adherence and regulatory compliance across multiple trial sites.

What they're looking for

  • Bachelor's degree in scientific or healthcare-related discipline
  • Extensive CRA experience with strong clinical trial process knowledge
  • Ability to manage multiple sites and projects simultaneously
  • Expertise in monitoring practices, data integrity, and clinical trial software
  • Strong communication and stakeholder management skills
  • Willingness to travel approximately 60% for site visits

What you'll be doing

  • Monitor clinical trial sites for protocol adherence and GCP standard compliance
  • Conduct site visits to assess performance, resolve issues, and provide operational support
  • Collaborate with cross-functional teams on timely and accurate data collection
  • Train site staff and other CRAs on clinical trial conduct standards
  • Build and maintain relationships with site personnel and stakeholders
CompensationCompetitive base salary and performance-related incentives

Privacy & handoff

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What RoleLantern checked

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RoleLantern checked active
RoleLantern checkedNeeds clarity
Date posted5 days ago
Last source checkToday
Salary listedNeeds clarity
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