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Clinical Data Manager

168 ICON Clinical Research Poland sp. z.o.o. · Warsaw, Poland

Clinical TrialsImported listingfull-time1 day ago

About The Role

Clinical Data Manager (ICON Job Title: Clinical Data Science Lead)

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.

As a Clinical Data Manager within ICON Strategic Solutions, you will be dedicated to one of our global pharmaceutical partners, working within a collaborative client-dedicated model. You will play a key role in delivering accurate, reliable, and inspection-ready clinical data that supports the development of innovative therapies for patients worldwide.

This is a hands-on opportunity for an experienced Clinical Data Manager who enjoys study ownership, data review, vendor collaboration and driving data quality from study start-up through database lock and close-out.

What You Will Be Doing

  • Lead or co-lead data management activities across assigned studies from start-up through close-out.
  • Perform EDC data review, data cleaning, query management and reconciliation of external data sources.
  • Create and maintain study documentation, including Data Management Plans, Data Review Plans, eCRF Completion Guidelines and Edit Check Specifications.
  • Conduct EDC and data validation listing UAT and support database lock readiness.
  • Partner with study teams and vendors to resolve data issues, including eCOA, PK, biomarker, local laboratory and safety data discrepancies.
  • Support SAE and protocol deviation reconciliation, issue log maintenance, metrics reporting and eTMF filing.

You will have/be

  • Bachelor's degree in a Life Sciences related discipline.
  • 5+ years of Clinical Data Management experience within a CRO, pharmaceutical or biotechnology environment.
  • Experience leading or co-leading studies from start-up through database lock and close-out.
  • Strong hands-on EDC review, data cleaning, query management, external data reconciliation and UAT experience.
  • Clear communication skills and the ability to work independently within fast-paced global study teams.
  • Veeva EDC experience is desirable but not essential.

#LI-RD1
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

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