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Clinical Research Coordinator, Pre-Clinical

🔥 0 minutes ago

🇬🇧 United Kingdom – Remote

⏰ Full Time

🟡 Mid-level

đźź  Senior

đź§Ş Clinical Research

đź‘» Ghost score 10%

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Logo of ICON plc

ICON plc

10,000+ employees

Founded 1990

đź’Ľ 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.

đź“‹ Description

• Co-ordinate the outsourcing and delivery of preclinical CPSS project activities • Support the development, maintenance, and interpretation of cross-functional project plans • Monitor timelines, budgets, resources, risks, and project deliverables • Facilitate communication and collaboration across project teams and stakeholders • Support management of external vendors and outsourced activities • Provide guidance on project management processes, tools, and best practices • Identify and help resolve day-to-day project challenges and risks • Communicate new processes, procedures, and strategies to project teams • Contribute to continuous improvement initiatives to enhance project delivery, quality, and efficiency

🎯 Requirements

• Bachelor's degree in a relevant scientific discipline • Experience in Scientific Project Management • Experience supporting pre-clinical drug development projects and activities • Strong organisational, planning, and communication skills • Ability to manage multiple priorities and work effectively within cross-functional teams • Understanding of scientific project management principles, including project planning, resource management, and risk management • Employment with ICON is contingent upon having the 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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