Senior Clinical Trial Manager

🔥 12 hours ago

🌐 United States, Canada – Remote

🇺🇸 United States – Remote 🇨🇦 Canada – Remote

🔔 Pennsylvania – Remote

🔔 Pennsylvania – Remote

⏰ Full Time

🟠 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

• Lead the operational delivery of assigned clinical trials, ensuring milestones, timelines, budget expectations, and quality standards are achieved • Drive study start-up activities, site activation, enrollment strategies, and study execution through database lock • Provide oversight of study progress, monitoring activities, clinical metrics, and site performance • Develop and implement effective study oversight plans, monitoring strategies, and risk mitigation approaches • Identify operational challenges and proactively implement solutions to ensure successful study delivery • Build and maintain strong relationships with sponsors, investigators, vendors, and cross-functional stakeholders • Review study performance metrics and provide regular status updates and reporting • Support, mentor, and collaborate with Clinical Research Associates (CRAs) and other study team members • Ensure all clinical trial activities comply with protocol requirements, ICH-GCP guidelines, and applicable regulatory requirements

🎯 Requirements

• Bachelor's degree in Life Sciences, Health Sciences, Nursing, Pharmacy, or another relevant scientific discipline, or an equivalent combination of education and experience • Significant Clinical Trial Management experience within a CRO (preferred), pharmaceutical, or biotechnology environment • Demonstrated ability to successfully lead and deliver clinical studies from start-up through closeout • Strong understanding of clinical trial operations, ICH-GCP, and applicable regulatory requirements • Experience managing study timelines, budgets, vendors, and cross-functional stakeholders • Proven ability to identify risks, solve complex operational challenges, and drive study execution • Prior monitoring experience preferred • Experience managing global and/or complex clinical trials preferred • Ability to travel up to 20% • 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