Clinical Trial Liaison

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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

• Support clinical trials by providing scientific and clinical support to investigators and site staff • Ensure study sites thoroughly understand study design and procedures • Help achieve clinical trial goals • Function as a recruitment specialist by developing and optimising site- and study-level strategies • Drive successful patient enrolment • Engage with sites and attend industry meetings and conferences • Drive strategies to widen patient access and execute them • Collaborate with medical and scientific leaders, advocates, and key decision makers across the ecosystem • Translate best practices into local tactical action • Cultivate relationships and recruit appropriate sites to participate in trials • Work collaboratively and independently while travelling up to approximately 75%

🎯 Requirements

• A scientific and clinical network and networking skills • Demonstrated success in persuasion, influence, and negotiation • Ability to discuss and apply technical, scientific, and clinical knowledge • Strong communication and presentation skills in local medical language(s) • Knowledge of the local healthcare landscape • Business, technical, and analytical skills • Willingness and flexibility to learn new therapeutic areas and products • Critical thinking and operational expertise • Fluency in English and the local country language • A doctoral degree, M.D., PharmD, or PhD is required • Experience in a clinical research environment in Pharma, Biotech, or CRO in scientific and/or clinical operations is preferred • Broad scientific and medical knowledge with an understanding of clinical development • Excellent interpersonal skills with the ability to develop relationships with internal and external stakeholders • Proactive and self-motivated, with the demonstrated ability to work collaboratively and independently • Ability to travel up to approximately 75% • Legal right to work in France

🏖️ 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 • Inclusive and accessible workplace • Reasonable accommodations during the recruitment process • Sustainable business practices and support for local communities