CRA II/Sr CRA - Sponsor Dedicated at ICON plc | GB | Rezi

CRA II/Sr CRA - Sponsor Dedicated at ICON plc

CRA II/Sr CRA - Sponsor Dedicated

ICON plc · GB

Yesterday

CRA II/Sr CRA - Sponsor Dedicated

ICON plc · GB

a day ago
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About the Role

As a Senior CRA at ICON Plc, you will oversee and manage clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement.

Responsibilities

  • Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
  • Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
  • Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting.
  • Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
  • Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations.

Requirements

  • Bachelor's degree in a relevant scientific discipline or healthcare-related field
  • Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
  • Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
  • Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
  • Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
  • Willingness to travel as required (approximately 60%)
  • Must be based in the UK
  • Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Skills

  • Clinical trial monitoring
  • Data integrity
  • Site management
  • Clinical trial software and tools
  • Communication
  • Interpersonal skills
  • Stakeholder management

Location

  • UK

Work Type

  • Fully sponsor dedicated

Experience Level

  • Sr CRA
  • CRA2

Education Level

  • Bachelor's degree in a relevant scientific discipline or healthcare-related field

Benefits

  • Competitive base salary and performance related incentives
  • Health and wellbeing programmes including medical, dental, and vision coverage where applicable
  • Retirement and pension plans
  • Life assurance and disability coverage
  • Employee assistance programmes and wellbeing resources
  • Learning and development opportunities through structured training and career pathways

About the Company

  • At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.
  • As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

Equal Opportunity

  • ICON is an equal opportunity employer.
  • We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
  • If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.