Clinical Scientist – Veeva EDC

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🔥 25 minutes ago

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

🇬🇧 United Kingdom – Remote 🇩🇪 Germany – Remote 🇧🇬 Bulgaria – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🧪 Clinical Research

👻 Ghost score 10%

What it means: the chance that no one is really hiring for this job.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

• Support the EDC transition, leveraging strong hands-on experience with Veeva EDC • Apply a clinical monitoring background to support clinical study activities, data quality, and operational requirements throughout the transition • Design and implement clinical trial protocols in accordance with scientific and regulatory standards • Conduct data analysis and interpretation to derive insights supporting study objectives • Collaborate with cross-functional teams to ensure effective study execution and data quality • Engage with stakeholders to communicate findings and contribute to scientific discussions

🎯 Requirements

• Bachelor's degree in a relevant scientific discipline or healthcare-related field • CRA/monitoring background with Veeva EDC experience are welcomed • Experience in clinical research or a related scientific role, with a strong understanding of clinical trial processes • Excellent analytical skills and proficiency in data interpretation and statistical analysis • Strong communication and collaboration skills, with the ability to work effectively in interdisciplinary teams • 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

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