Global Study Manager

🔥 3 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

• Collaborate with cross-functional teams to design and implement effective clinical trial enrollment • Develop and implement comprehensive clinical trial protocols • Oversee and manage the day-to-day operations of clinical trials • Ensure compliance with regulatory standards • Analyze and interpret clinical trial data, identify trends, and provide insights to optimize study outcomes • Proactively address challenges and implement effective solutions to ensure successful clinical trial execution • Communicate with internal and external stakeholders to foster strong partnerships and facilitate smooth trial processes

🎯 Requirements

• Bachelor's degree in a relevant field • Minimum of 5 years of experience in global clinical trial management • Proven expertise in designing and executing clinical trials • Strong understanding of regulatory requirements • Exceptional analytical and problem-solving skills • Ability to interpret complex medical data • Effective communication and interpersonal skills • Ability to collaborate across diverse teams • Detail-oriented and organized • Track record of successfully managing multiple tasks and priorities simultaneously • 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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