Global Study Manager

🔥 16 minutes ago

🌐 Canada, United States – Remote

🇨🇦 Canada – Remote 🇺🇸 United States – 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

• Coordinate clinical trial management delivery, resolve issues, and develop team capability • Oversee the planning, execution, and monitoring of clinical trials to ensure compliance with regulatory requirements and project timelines • Collaborate with investigators, vendors, and internal stakeholders to implement clinical studies successfully • Develop and manage study budgets, resources, and timelines • Lead resolution of issues and challenges arising during clinical trials • Ensure data integrity and quality through monitoring and validation processes throughout the study lifecycle

🎯 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

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