Senior Clinical Scientist – Single Client Dedicated

Job not on LinkedIn

🕒 September 3

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

🇬🇧 United Kingdom – Remote 🇪🇸 Spain – Remote 🇵🇱 Poland – Remote

⏰ Full Time

🟠 Senior

🧪 Clinical Research

👻 Ghost score 24%

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

• Provide strategic leadership and demonstrate accountability for clinical programs supporting early clinical development and clinical pharmacology • Maintain knowledge of the competitive landscape, current assets, and evolving standards of care • Provide subject matter expertise on cross-functional project teams • Author, review, and approve clinical protocols, analysis plans, study reports, and regulatory submissions • Execute Clinical and Clinical Pharmacology studies in collaboration with Clinical Operations • Review and summarize clinical safety or efficacy data with the Medical Monitor • Collaborate with Quantitative Clinical Pharmacology, Translational Sciences, and Statistics to develop protocols and summarize analysis • Contribute to program strategy and clinical development plans for assigned compounds/programs • Draft and review clinical scientific documents, including INDs, IND amendments, Investigator Brochures, Annual Reports, and Health Authority submissions • Ensure adherence to timelines and budgets for accurate execution of clinical study and program deliverables

🎯 Requirements

• At least 5 years’ experience and a PhD, PharmD or MD degree • Or at least 10 years’ experience with BS/MS degree with emphasis on early development, clinical pharmacology or a related discipline • Early phase/Phase I experience required • Experience in clinical pharmacology, immunology or oncology is preferred • Ability to critically analyze problems and provide creative solutions • 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