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Clinical Data Manager

Job in Swansea, Swansea County, SA1, Wales, UK
Listing for: Icon Clinical PLC
Full Time position
Listed on 2026-09-14
Job specializations:
  • IT/Tech
    Information Security & Data Protection, Data Analyst
Job Description & How to Apply Below
Senior 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  at ICON, you will be client dedicated, serving as the primary data lead across global clinical trials and partnering closely with sponsors to drive high-quality, regulatory-compliant data delivery from study start-up through database lock.

Key responsibilities

Acting as the primary data lead within cross-functional study teams and sponsor partnerships

Driving study start-up activities including EDC build, system integrations, UAT, and key data management deliverables

Overseeing data review, reconciliation, vendor management, and database lock activities

Ensuring compliance with CDISC standards, ICH-GCP requirements, and regulatory expectations

Identifying and mitigating risks while driving continuous improvement and operational excellence

You will Have/Be:

Bachelor's degree in Life Sciences, Health Sciences, or a related discipline6+ years of Clinical Data Management or Clinical Data Science experience within a CRO or pharmaceutical environment

Proven experience leading studies across the full clinical trial lifecycle

Experience as a primary Data Lead on complex studies and/or extensive hands-on data review and reconciliation experience across EDC, vendor, eCOA, IRT, and SAE data Strong vendor oversight and stakeholder management experience

Hands-on experience with EDC systems, with Veeva EDC preferred

Knowledge of CDISC standards, including SDTMStrong understanding of clinical trial processes, regulatory requirements, and ICH-GCPExcellent communication, problem-solving, and project leadership skills

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & BenefitsICON 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 AccessibilityICON 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  to apply

Summary

Location:

Poland, Warsaw; UK, Livingston; UK, Reading;
South Africa, Johannesburg; UK, Swansea Type:
Full time
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