Clinical Trial Manager – Project Lead

🔥 12 hours ago

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ICON plc

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1990

💊 Pharmaceuticals

🧬 Biotechnology

⚕️ Healthcare Insurance

Pharmaceuticals • Biotechnology • Healthcare Insurance

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

• Manage day-to-day clinical trial management activities, supporting your team to deliver quality outcomes. • Plan and manage all aspects of clinical trials, ensuring adherence to timelines, budget, and quality standards. • Collaborate with cross-functional teams to establish and implement clinical trial protocols and procedures. • Train and mentor new CTA and LCRA staff. • Assign work across the team. • Monitor the progress of deliverables. • Run, review, and analyze reports for accuracy and work with the project teams to ensure updates are completed correctly. • Prepare reports on the status of deliverables and Hub progress to be presented to the project teams.

🎯 Requirements

• University degree in medicine, science, or equivalent combination of education & experience • 5+ years in clinical research, with substantial experience in clinical trial management, project management, or related roles. • Proven experience in leading study teams, managing cross-functional teams, or supervising junior CTMs and CRAs • Strong understanding of GCP, ICH guidelines, FDA regulations, and other relevant global regulatory requirements • Proficiency in CTMS, EDC, eTMF, and systems like Veeva Vault, Oracle, and Medidata • Experience in managing study budgets, forecasting resources, and coordinating with finance or procurement for trial supplies. • Ability to develop and manage project plans, timelines, and milestone tracking • Experience in managing third-party vendors, such as CROs, labs, and other service providers.

🏖️ 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