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ICON plc

Clinical Data Manager

Posted 19 Days Ago
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In-Office
Livingston, West Lothian, Scotland, GBR
Senior level
In-Office
Livingston, West Lothian, Scotland, GBR
Senior level
Leads clinical data management across global trials from study start-up through database lock. Responsibilities include EDC builds, system integrations, UAT, data review and reconciliation, vendor oversight, regulatory compliance, risk mitigation, and stakeholder management. The role serves as the primary data lead for complex studies and requires expertise in CDISC standards, SDTM, ICH-GCP, clinical trial processes, and multiple clinical data systems.
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Senior Clinical Data Manager

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 Clinical Data Manager  at ICON, you will be client dedicated, serving as the primary data lead across global clinical trials and partnering closely with sponsors to drive high-quality, regulatory-compliant data delivery from study start-up through database lock.

Key responsibilities

  • Acting as the primary data lead within cross-functional study teams and sponsor partnerships
  • Driving study start-up activities including EDC build, system integrations, UAT, and key data management deliverables
  • Overseeing data review, reconciliation, vendor management, and database lock activities
  • Ensuring compliance with CDISC standards, ICH-GCP requirements, and regulatory expectations
  • Identifying and mitigating risks while driving continuous improvement and operational excellence

You will Have/Be:

  • Bachelor's degree in Life Sciences, Health Sciences, or a related discipline
  • 6+ years of Clinical Data Management or Clinical Data Science experience within a CRO or pharmaceutical environment
  • Proven experience leading studies across the full clinical trial lifecycle
  • Experience as a primary Data Lead on complex studies and/or extensive hands-on data review and reconciliation experience across EDC, vendor, eCOA, IRT, and SAE data
  • Strong vendor oversight and stakeholder management experience
  • Hands-on experience with EDC systems, with Veeva EDC preferred
  • Knowledge of CDISC standards, including SDTM
  • Strong understanding of clinical trial processes, regulatory requirements, and ICH-GCP
  • Excellent communication, problem-solving, and project leadership skills

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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