Clinical Trial Manager

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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

• Act as the Functional Lead from Clinical Operations for delivery of all Clinical Operations aspects of clinical studies • Ensure consistency with ICON SOPs, study contracts and budgets • Build a culture of process improvement focused on streamlining processes, adding business value, and meeting client needs • Serve as the primary point of contact for Clinical Operations aspects of designated projects • Develop successful working relationships with clients • Plan, schedule, and implement project activities • Contribute to development and maintenance of cross-functional project management plans • Lead risk mitigation strategies, action plans, and issue resolution • Lead the Clinical Operations project team • Ensure necessary project training is provided to assigned staff • Provide direction and support to the study team • Collaborate with Business Development to ensure timely completion of change orders • Track project deliverables using appropriate tools

🎯 Requirements

• More than 8 years of professional experience in the clinical research field • At least 2 years of clinical project management experience • Experience managing sites • In-depth knowledge of local requirements and regulations across APAC countries, including China • Bachelor's degree in a science or medical area • Ability to communicate well • Understanding of compliance • Confidence to obtain funding • Strong interpersonal skills • Good command of written and spoken English • Computer literacy

🏖️ Benefits

• Very competitive salary packages • Annual bonuses reflecting delivery of performance goals • Health-related benefits for employees and their families • Competitive retirement plans • Life assurance • 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