Project Manager

November 26

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ICON plc

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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.

10,000+ employees

Founded 1990

💊 Pharmaceuticals

🧬 Biotechnology

⚕️ Healthcare Insurance

📋 Description

• Leading the regional clinical operations team effectively and act as point of escalation for resolution of issues within the region for the assigned studies • Leading external vendors involved in study delivery on a regional level • Planning and management of the assigned clinical studies from feasibility through closeout activities for region, in line with global study timelines • Ensure that the clinical study is operationally feasible in the region, drives trial feasibility, country allocation and site selection process for assigned region in collaboration with feasibility managers, country heads, medical affairs and any other stakeholders • Providing regional input on global study plans • Collaborating closely with CRAs in the region to ensure proper study execution at the sites. • Review and signs-off of monitoring reports • Monitoring study activities in region to ensure compliance with the study protocol, SOPs, ICH/GCP and all other relevant regulations • Working with the sourcing team to select and manage regional study vendors • Managing regional study budgets

🎯 Requirements

• University Degree in a scientific or healthcare discipline required • 4 or more years of progressive experience in clinical research within biotech, pharma or CRO industry • Strong experience in managing oncology studies is required • Proven experience in clinical research including relevant experience as team lead in clinical functions • Prior experience as CRA • Computer Skills: MS Office, Project Planning Applications

🏖️ Benefits

• Various annual leave entitlements • A range of health insurance offerings to suit you and your family’s needs. • Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead. • Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being. • Life assurance • Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.