10,000+ employees
Founded 1990
đŒ Consulting
đ„ Healthcare
đŠ Logistics
Consulting âą Healthcare âą 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.
đ„ 17 hours ago
đ Serbia, Spain, +6 more countries â Remote
â° Full Time
đ Senior
âš Clinical Liaison
đ» Ghost score 10%
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10,000+ employees
Founded 1990
đŒ Consulting
đ„ Healthcare
đŠ Logistics
Consulting âą Healthcare âą 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.
âą Lead CTL activities on studies employing multiple CTLs, coordinating workstreams and supporting delivery to expected quality and timelines âą Manage, mentor, train and coach CTL team members and other colleagues, supporting continued career development within the division and ICON âą Build a strong understanding of the scientific basis of assigned clinical trials and communicate complex scientific, protocol and study information clearly to project teams, investigators and site staff âą Create educational materials that effectively communicate the science behind the clinical trial and support consistent site understanding âą Build trusted relationships with investigators and site personnel to facilitate effective study conduct and site engagement âą Identify scientific and operational barriers affecting recruitment, retention and data quality, and work with study teams to address them âą Identify effective pre-screening strategies for each trial and recommend practical improvements based on site feedback and patient pathways âą Provide detailed, timely reports of interactions with investigators and site staff, including relevant insights for project teams âą Contribute to tools, materials and strategies that support site engagement and performance âą Participate in business development activities and represent the CTL function as assigned
âą Doctoral-degree level qualification such as a PhD, MD or PharmD in a relevant scientific, medical, pharmacy or healthcare discipline âą Substantial experience in clinical research, medical affairs or field-based roles involving direct interaction with investigators and clinical trial sites âą Strong understanding of clinical trial design, Good Clinical Practice (GCP) and site operations âą Ability to interpret complex medical and scientific information and explain protocol concepts clearly to different audiences âą Proven relationship-building skills and credibility with clinicians, investigators and site teams âą Demonstrated leadership and people-management capability, including experience coaching, mentoring and developing others âą Excellent communication, presentation, influencing and problem-solving skills âą Ability to manage competing priorities and work effectively in a matrixed, global environment âą Legal right to work in the country where the role is based
âą Competitive base salary and performance related incentives âą Health and wellbeing programmes including medical, dental, and vision coverage where applicable âą Retirement and pension plans âą Life assurance and disability coverage âą Employee assistance programmes and wellbeing resources âą Learning and development opportunities through structured training and career pathways
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