Clinical Data Manager

🔥 0 minutes ago

🌐 Poland, United Kingdom, +1 more countries – Remote

🇵🇱 Poland – Remote 🇬🇧 United Kingdom – Remote 🇿🇦 South Africa – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🧪 Clinical Research

👻 Ghost score 10%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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ICON plc

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1990

💼 Consulting

🏥 Healthcare

📦 Logistics

Consulting • Healthcare • Logistics

ICON plc is a global provider of clinical, consulting, and commercial services across various sectors in the healthcare and pharmaceutical industries. They offer a wide range of clinical solutions, including decentralised clinical trials, cardiac safety solutions, early clinical laboratories, and medical imaging. ICON also provides technology solutions that support drug development from early phases to post-marketing. Their therapeutic expertise spans cardiovascular, oncology, internal medicine, and more, with a strong focus on transformative therapies like cell and gene therapies and biosimilars. ICON is recognized as a leading Contract Research Organisation (CRO), regularly providing thought leadership and contributing to industry publications and events. Their services are tailored to optimize clinical trials, offer regulatory intelligence, and deliver real-world evidence through robust data analysis and patient-centric solutions.

📋 Description

• 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 • Work within a collaborative client-dedicated model for a global pharmaceutical partner

🎯 Requirements

• 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 • Employment contingent upon having the legal right to work in the country where the role is based • Veeva EDC experience is desirable but not essential

🏖️ Benefits

• 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