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ICON plc

Clinical Data Manager – II

ICON plc

Clinical Data Manager overseeing clinical data science workstreams for ICON. Responsible for data management strategies, collaboration with teams, and compliance with regulatory requirements.

Posted 7/9/2026full-timeRemote • 🇬🇧 United KingdomSeniorLeadWebsite

Core Competencies

Role fit
Core Competencies

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Demonstrates expertise in clinical data management, including data governance, quality control, and compliance with regulatory requirements. Proven ability to lead cross-functional teams and manage clinical data science workstreams to optimize data collection and analysis.

Highest-signal resume keywords
Clinical Data ManagementData Analysis ToolsLeadership SkillsStakeholder ManagementUser Acceptance Testing

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Clinical Data ManagementData ReviewData Quality ProcessesStatistical SoftwareData VisualizationChange Control ActivitiesDatabase Lock ManagementReal Time Data ExtractionDose Escalation StudiesClinical Trial Design
Soft Skills
Excellent CommunicationProblem SolvingProactive Approach
Industry Keywords
Life SciencesClinical ResearchCRO OversightEarly DevelopmentPhase I Studies

About the role

Key responsibilities & impact
  • You will oversee clinical data science workstreams, ensuring deliverables meet quality and timeline expectations
  • Leading the development and implementation of clinical data management strategies to optimize data collection, analysis, and reporting
  • Collaborating with cross-functional teams to ensure the accurate integration of data science techniques into clinical trial designs
  • Overseeing the analysis of clinical data to provide actionable insights that inform study decisions and outcomes
  • Providing strategic guidance on data governance, quality control, and compliance with regulatory requirements
  • Establishing partnerships with key stakeholders to leverage the latest advancements in data science and technology in clinical research

Requirements

What you’ll need
  • Bachelor's degree in Life Sciences, Computer Science, or a related field
  • 8 to 10 years of clinical data management experience, including Early Development and Phase I studies
  • Experience leading at least three study start ups and three database locks
  • Strong knowledge of clinical data management, data review, and data quality processes
  • Experience participating in User Acceptance Testing and reviewing data reports
  • Comfortable managing frequent real time data extractions and supporting rapid study decisions
  • Experience leading post production changes and change control activities
  • Experience overseeing Clinical Data Coordinators and delegated activities
  • Experience managing external data vendors and third party data deliverables
  • Exposure to dose escalation studies and meetings preferred
  • Strong leadership skills with experience working across cross functional teams
  • Proficient in data analysis tools, statistical software, and data visualization
  • Excellent communication, stakeholder management, and problem solving skills
  • Proactive approach with the confidence to research, resolve issues, and drive outcomes
  • CRO oversight experience preferred but not required
  • Willingness to travel up to 15 percent as required

Benefits

Comp & perks
  • 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