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The Senior Clinical Data Lead oversees the management and analysis of clinical trial data to ensure accuracy, integrity, and regulatory compliance. They also provide strategic guidance on data practices and mentor data teams to drive continuous improvement.

Senior Clinical Data Lead

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 Senior Clinical Data Lead at ICON, you will be instrumental in overseeing the management and analysis of clinical trial data to ensure the accuracy, integrity, and efficiency of data processes.

What You Will Do:

You will manage day-to-day scientific operations activities, supporting your team to deliver quality outcomes.

Key responsibilities include:

  • Leading the management and analysis of clinical trial data, ensuring high standards of data accuracy, integrity, and regulatory compliance.
  • Collaborating with cross-functional teams to design and implement data strategies that support clinical research objectives and optimize data workflows.
  • Overseeing data collection, processing, and validation to ensure consistency and reliability across clinical trials.
  • Providing strategic guidance on data management practices, including the development of data analysis plans and reporting methodologies.
  • Managing and mentoring data teams, fostering a collaborative environment to drive continuous improvement in data handling and analysis.

Your Profile:

You will have solid scientific operations experience, with the ability to manage competing priorities and develop your team.

Required qualifications and experience:

  • Bachelor's degree in life sciences, computer science, or a related discipline
  • Extensive experience in clinical data management and analysis, with a deep understanding of clinical trial processes and regulatory requirements.
  • Proven leadership skills with the ability to manage and develop data teams, and drive data quality initiatives.
  • Expertise in data analysis and statistical methodologies, with proficiency in relevant software and programming languages.
  • Excellent communication and interpersonal skills, with a demonstrated ability to collaborate effectively with cross-functional teams and stakeholders.
  • Willingness to travel as required (approximately 10%)

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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