Clinical Study Manager

🔥 1 hour ago

🌐 Spain, Romania, +2 more countries – Remote

🇪🇸 Spain – Remote 🇷🇴 Romania – Remote 🇧🇬 Bulgaria – Remote 🇬🇧 United Kingdom – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🧪 Clinical Research

👻 Ghost score 10%

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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

• Oversee the planning, execution, and monitoring of clinical trials to ensure compliance with regulatory requirements and project timelines • Collaborate with cross-functional teams, including investigators, vendors, and internal stakeholders, to drive the successful implementation of clinical studies • Develop and manage study budgets, resources, and timelines, ensuring efficient use of resources and adherence to study plans • Lead the resolution of issues and challenges that may arise during clinical trials, employing effective problem-solving skills and communication strategies • Ensure data integrity and quality by implementing rigorous monitoring and validation processes throughout the study lifecycle • Design and analyze clinical trials, interpret complex medical data, and contribute to the advancement of innovative treatments and therapies • Coordinate clinical trial management delivery, resolve issues, and develop team capability

🎯 Requirements

• Bachelor's degree in a relevant scientific discipline or healthcare-related field • Proven experience in clinical study management, with a strong understanding of the drug development process and regulatory requirements • Excellent project management skills, including the ability to handle multiple tasks simultaneously and prioritize effectively • Strong communication and interpersonal skills, with the ability to collaborate effectively with cross-functional teams and external partners • Detail-oriented with a focus on ensuring data accuracy and maintaining high-quality standards in clinical trials • 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