ICON plc
ICON plc
ICON plc is a global contract research organisation serving the healthcare and pharmaceutical industries. Its work spans clinical, consulting, and commercial services that support drug development from early research through post-marketing activities. The company provides solutions including decentralised clinical trials, cardiac safety, early clinical laboratories, medical imaging, regulatory intelligence, and real-world evidence. ICON plc also brings therapeutic expertise to areas such as cardiovascular disease, oncology, internal medicine, cell and gene therapies, and biosimilars, combining data analysis with patient-focused approaches to help advance clinical programmes.

Senior Clinical Data Manager, Data Standards

Lead clinical data standards, quality, and governance for ICON’s sponsor-dedicated trials. Improve global processes and coordinate delivery across teams.

Description

  • Lead the development and implementation of clinical data standards processes and best practices.
  • Drive work on data cleaning, data quality, edit checks, data listings, and standards library management.
  • Work closely with Clinical Trial Reporting (CTR), Clinical Trial Configuration (CTC), and Cross-Functional Data Review (CFDR) teams.
  • Set governance, workflows, and quality standards that support clinical trial delivery.
  • Lead and mentor Associate Manager-level colleagues and encourage continuous improvement.
  • Work with cross-functional stakeholders to turn strategic objectives into operational plans.
  • Identify risks, improve processes, and advance data quality throughout the clinical data lifecycle.

Requirements

  • Hold a bachelor’s degree in life sciences, health sciences, or a related field.
  • Bring extensive clinical data management experience from a CRO, biotechnology, or pharmaceutical setting.
  • Have strong experience in process development, project management, stakeholder engagement, and cross-functional collaboration.
  • Show a proven ability to build and implement new processes and ways of working.
  • Have experience with data quality, standards development, data review, edit checks, data listings, or standards library management.
  • Understand clinical trial processes, regulatory requirements, and ICH-GCP.
  • Demonstrate strong communication, problem-solving, and leadership skills.
  • Bring an entrepreneurial outlook and the ability to thrive in a developing, evolving function.
  • Have legal authorization to work in the country where the role is based.

Benefits

  • Competitive base pay with 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 through structured training and career pathways.

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