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Manager, Clinical Operations

🔥 0 minutes ago

🇬🇧 United Kingdom – Remote

⏰ Full Time

🟡 Mid-level

đźź  Senior

🏥 Clinical Operations

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

• Manage day-to-day clinical trial management activities, supporting the team to deliver quality outcomes • Manage overall operational aspects of clinical trial projects from study initiation through close-out • Collaborate with cross-functional teams to develop study plans, timelines, and budgets • Oversee Clinical Trial Managers and study teams, providing guidance and support • Ensure compliance with regulatory requirements, Good Clinical Practice (GCP), and internal policies • Identify risks and implement mitigation strategies for successful clinical trial delivery • Develop the team and manage competing priorities

🎯 Requirements

• Degree in life sciences, clinical research, or a related field • Significant experience in clinical trial management, with a proven track record of leading successful trials • Strong understanding of regulatory requirements and GCP in clinical research • Excellent leadership and communication skills, with the ability to motivate and manage cross-functional teams • Proven analytical and problem-solving skills, capable of navigating complex project challenges • Willingness to travel as required (approximately 25%) • 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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