HiredNow AI
ICON

Senior Clinical Data Manager

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Found by HiredNow AI on 30 Sept 2026. Subscribers saw it first.

About the role

Senior Clinical 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 Clinical Data Science Lead at ICON, you will drive data science initiatives within clinical trials, ensuring that our analyses provide meaningful insights that inform strategic decisions.

Key Responsibilities

  • Serve in a support‐level capacity on a Clinical Data Management team to provide efficient and quality clinical data management products. Support the design, specifications, and development of eCRFs, ensuring adherence to company standards.
  • Coordinate the development and testing of clinical data management systems edit checks and listings/reports/tools for data review and discrepancy management activities.
  • Support the development of Data Management Plan documents that will ensure delivery of accurate, timely, consistent, and high‐quality clinical data. Works with Third Party /External data Vendors to complete the set‐up of data import and reconciliation processes.
  • Perform comprehensive review of all data generated from the clinical study including Third Party/External data, SAE data and local lab data, as applicable. Oversees quality control procedures. Develop and maintain strong communications and working relationships with CDM team.
  • Effectively manage project timelines and quality.
  • Provide reports, status updates, feedback, and advice to key study stakeholders on the progress of data cleaning and risk identification/mitigation activities.
  • Ensure CDM activities are performed in compliance with Good Clinical Practice, ICH Guidelines.
  • Apply appropriate best practices and independently offer project solutions to the study team.
  • Support the filing of eTMF documentation to ensure that an inspection ready environment is maintained throughout the study lifecycle.
  • Provide back up support for Principal Clinical Data Lead as required.
  • Your Profile: 4+ years of Clinical Data Management experience
  • Ability to work under pressure demonstrating agility through effective and innovative team leadership
  • Robust experience with EDC (E.g. Medidata Rave) and use of Data Review tools such as elluminate, J‐Review or Business Objects required

Experience in Phase I/II

  • Neurology experience would be desirable.
  • Extensive experience in Study startup.
  • Strong technical skills, including experience working with using Microsoft Excel functionality
  • Fluent English (oral and written)
  • Strong understanding of drug development and biopharmaceutical industry required.
  • High attention to detail including proven ability to manage multiple, competing priorities
  • Excellent written and oral communication skills
  • #LI-JC3
  • #LI-Remote
  • 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
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  • Are you a current ICON Employee? Please click here to apply
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