Global Study Manager

🔥 0 minutes ago

🇬🇧 United Kingdom – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

👔 Manager

👻 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

• Support the delivery of Cell Therapy global clinical studies from protocol development through study close-out and archiving • Collaborate with internal stakeholders, CROs, and external vendors as part of a cross-functional global study team • Ensure studies are delivered on time, within budget, and to the highest quality and compliance standards • Support innovative programmes, including global cardiovascular clinical trials focused on advancing treatments for patients with cardiovascular disease • Play a key role in global studies, including those within the cardiovascular therapeutic area

🎯 Requirements

• Degree qualified in Life Sciences, Medical Sciences, Biological Sciences, or a related field • 3+ years of experience in clinical research, pharmaceutical development, biotechnology, or a CRO environment • Strong understanding of clinical development and the drug development process • Excellent knowledge of ICH-GCP and global clinical trial regulations • Proven project management and organisational skills • Strong stakeholder management and communication skills • Experience working effectively within global, cross-functional teams • Previous experience supporting cardiovascular clinical trials is highly desirable • Proactive, collaborative, and able to work independently in a fast-paced environment • 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