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ICON plc logo

ICON plc

Lead Data Manager

Lead Data Manager

United KingdomRemote
Permanent

Lead Data Manager

ICON plc

Full-Time
Sign up to unlock the estimation.Sign up to unlock the estimation~£60,000 - £75,000per annum· Meev estimate

Posted 6 days ago

Description

Lead Data Manager
At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.

As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

As a Lead Data Manager at ICON, you will drive data science initiatives within study start up clinical trials, ensuring that our analyses provide meaningful insights that inform strategic decisions.

What You Will Do:
You will manage day-to-day clinical data science activities, supporting your team to deliver quality outcomes.

Key responsibilities include:
  • Lead end-to-end clinical data management start-up activities from protocol review through specification development, database build, testing, validation, and production go-live.
  • Review draft and approved protocols to identify data collection requirements, build risks, inconsistencies, and potential impacts to database design or downstream processes.
  • Translate protocol requirements into complete and accurate study build specifications, including visit schedules, assessments, eCRFs, dosing, data collection requirements, and edit check specifications.
  • Apply clinical data standards, including CDISC standards, eCRF design principles, field and variable conventions, and approved standard forms, to ensure consistent and compliant study configuration.
  • Partner with the Standards team to leverage existing standards and define, document, and implement protocol-specific modifications when needed.
  • Collaborate with Study Execution Teams (SET), Medical Data Review (MDR), Programming, Data Management, Standards, and other cross-functional stakeholders to clarify requirements, resolve discrepancies, and coordinate study configuration activities.
  • Plan, coordinate, and oversee sandbox testing and user acceptance testing (UAT), including documentation of defects, issue resolution, retesting, and confirmation of system readiness.
  • Manage start-up timelines, dependencies, deliverables, risks, and issue-resolution activities to ensure timely and successful database go-live.
  • Assess and manage the data management impact of protocol amendments and post–go-live changes, including updates to specifications, system configuration, testing, validation, and documentation.
  • Maintain complete, accurate, and timely data management start-up documentation in the eTMF.
  • Ensure all data management start-up deliverables comply with applicable SOPs, ICH-GCP, regulatory requirements, and internal quality standards.

Your Profile:
You will have solid clinical data 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 data analysis and project leadership within a clinical research setting.
  • Strong expertise in statistical software and data visualization techniques.
  • Exceptional analytical and problem-solving skills, with a focus on translating data into actionable insights.
  • Excellent communication and leadership skills, with the ability to foster collaboration across diverse teams.
  • Willingness to travel as required (approximately 15%)

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
ICON plc cover
ICON plc logo

ICON plc

A world leading clinical research organisation accelerating drug and device development globally

DublinContract Research1000+
ICON plc logo

ICON plc

Contract Research

Shape the future of healthcare by working at the forefront of clinical research innovation, where your expertise directly accelerates life saving treatments for patients worldwide through cutting edge AI, real world data, and global collaboration.

Click to learn more
ICON plc logo

ICON plc

Contract Research

Shape the future of healthcare by working at the forefront of clinical research innovation, where your expertise directly accelerates life saving treatments for patients worldwide through cutting edge AI, real world data, and global collaboration.

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