Senior Clinical Scientist

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ICON plc

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 with Clinical Operations • Review and summarize clinical safety and efficacy data with the Medical Monitor • Collaborate with Quantitative Clinical Pharmacology, Translational Sciences, and Statistics to develop protocols and summarize analyses • Contribute to program strategy for assigned compounds and programs, including clinical development plans • Draft and review INDs, IND amendments, Investigator Brochures, Annual Reports, and other Health Authority submissions • Ensure adherence to timelines, budgets, scientific standards, regulatory requirements, and SOPs • Develop collaborative relationships with consultants and external experts • Participate in project teams and liaise with project teams, CROs, Clinical sub-teams, and other stakeholders • Present data at internal and external scientific meetings • Author manuscripts for scientific journals

🎯 Requirements

• At least 5 years’ experience with a PhD, PharmD, or MD degree • Alternatively, at least 10 years’ experience with a BS/MS degree emphasizing early development, clinical pharmacology, or a related discipline • Experience in early development, clinical pharmacology, or a related discipline • Ability to critically analyze problems and provide creative solutions • Excellent written and oral communication skills • Ability to present to and influence matrix teams and senior leaders • Ability to work independently and manage multiple priorities in a dynamic environment • Experience in clinical pharmacology, immunology, or oncology preferred • Early phase/Phase I experience required • Willingness to travel up to 20% • Legal right to work in the country where the role is based • Ability to work in compliance with departmental and organizational SOPs, scientific standards, and regulatory requirements

🏖️ 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 • Accommodations available for individuals with disabilities • Reasonable accommodations during the recruitment process • Opportunity to contribute to a diverse, inclusive, and accessible workplace • Opportunity to make a difference to patients’ lives • Sustainable business practices and community support

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