Clinical Data Manager

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