Senior Director, Clinical Systems at ICON plc | Dublin, Dublin, IE | Rezi

Senior Director, Clinical Systems at ICON plc

Senior Director, Clinical Systems

ICON plc · Dublin, Dublin, IE

1 months ago

Senior Director, Clinical Systems

ICON plc · Dublin, Dublin, IE

a month ago
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About the Role

As a Senior Director, Clinical Systems at ICON Plc, you will oversee the development, implementation, and management of clinical systems and technologies, directing scientific operations activities to ensure quality, efficiency, and alignment with business objectives.

Responsibilities

  • Lead the strategic planning, development, and implementation of clinical systems, including Electronic Data Capture (EDC), Clinical Trial Management Systems (CTMS), and other technologies supporting clinical trials.
  • Oversee the integration and optimization of clinical systems to ensure seamless data flow, operational efficiency, and compliance with regulatory standards.
  • Collaborate with cross-functional teams, including clinical operations, data management, and IT, to define system requirements, address operational challenges, and drive continuous improvement.
  • Provide strategic direction on system selection, implementation, and maintenance, ensuring alignment with study objectives, data quality standards, and organizational goals.
  • Stay abreast of industry trends and technological advancements to drive innovation in clinical systems and enhance trial management and data analysis capabilities.

Requirements

  • Bachelor's degree in a relevant scientific discipline or healthcare-related field; advanced degree preferred.
  • Extensive experience in managing clinical systems, with a proven track record of overseeing the implementation and optimization of EDC, CTMS, and other clinical technologies.
  • Strong leadership skills with experience in strategic planning, project management, and cross-functional collaboration within the clinical research environment.
  • Expertise in system integration, data management, and regulatory compliance, with a deep understanding of clinical trial processes and industry best practices.
  • Excellent communication, organizational, and problem-solving skills, with the ability to present complex information clearly, influence decision-making, and build strong relationships with internal and external stakeholders.
  • Willingness to travel as required (approximately 10%).
  • Must have the legal right to work in the country where the role is based.

Skills

  • Electronic Data Capture (EDC)
  • Clinical Trial Management Systems (CTMS)
  • System integration
  • Data management
  • Regulatory compliance
  • Strategic planning
  • Project management
  • Cross-functional collaboration
  • Communication
  • Organizational skills
  • Problem-solving

Experience Level

  • Senior

Education Level

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

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

  • 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.

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.