Clinical Data Manager

🕒 September 7

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

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

⏰ Full Time

🟡 Mid-level

🟠 Senior

🧪 Clinical Research

👻 Ghost score 19%

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

• Act as the primary data lead within cross-functional study teams and sponsor partnerships • Drive study start-up activities including EDC build, system integrations, UAT, and key data management deliverables • Oversee data review, reconciliation, vendor management, and database lock activities • Ensure compliance with CDISC standards, ICH-GCP requirements, and regulatory expectations • Identify and mitigate risks while driving continuous improvement and operational excellence • Serve as the primary data lead across global clinical trials and partner closely with sponsors to drive high-quality, regulatory-compliant data delivery from study start-up through database lock

🎯 Requirements

• Bachelor's degree in Life Sciences, Health Sciences, or a related discipline • 6+ 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 SDTM • Strong understanding of clinical trial processes, regulatory requirements, and ICH-GCP • Excellent communication, problem-solving, and project leadership skills • Legal right to work in the country where the role is based

🏖️ 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