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ICON plc

Manager, Clinical Operations

Posted a day ago
5-10 years experience
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You will manage the operational aspects of clinical trials from initiation to close-out while ensuring compliance with regulatory standards and GCP. Additionally, you will lead and support cross-functional teams to deliver quality outcomes within established timelines and budgets.

Clinical Trial Manager - UK based - remote working

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.


As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.


As a Manager, Clinical Trial Management at ICON, you will oversee the planning and execution of clinical trials, ensuring that they are conducted efficiently and in compliance with regulatory standards.

What You Will Do:

You will manage day-to-day clinical trial management activities, supporting your team to deliver quality outcomes.

Key responsibilities include:

  • Managing the overall operational aspects of clinical trial projects, from study initiation through to close-out.
  • Collaborating with cross-functional teams to develop study plans, timelines, and budgets, ensuring alignment with project goals.
  • Overseeing the performance of Clinical Trial Managers and study teams, providing guidance and support as needed.
  • Ensuring compliance with regulatory requirements, Good Clinical Practice (GCP), and internal policies throughout the trial process.
  • Identifying risks and implementing strategies to mitigate them, ensuring the successful delivery of clinical trials.

Your Profile:

You will have solid clinical trial management experience, with the ability to manage competing priorities and develop your team.

Required qualifications and experience:

  • Degree in life sciences, clinical research, or a related field.
  • Significant experience in clinical trial management, with a proven track record of leading successful trials.
  • Strong understanding of regulatory requirements and GCP in clinical research.
  • Excellent leadership and communication skills, with the ability to motivate and manage cross-functional teams.
  • Proven analytical and problem-solving skills, capable of navigating complex project challenges.
  • Willingness to travel as required (approximately 25%)

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.


Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.


Benefits may include:

  • 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

Benefits may vary depending on role and location.


Visit our careers site to read more about the benefits ICON offers.


Inclusion and Accessibility

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.

Are you a current ICON Employee? Please click here to apply

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