Lead, Clinical Trial Liaison

đŸ”„ 17 hours ago

🌐 Serbia, Spain, +6 more countries – Remote

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⏰ Full Time

🟠 Senior

✹ Clinical Liaison

đŸ‘» Ghost score 10%

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Logo of ICON plc

ICON plc

10,000+ employees

Founded 1990

đŸ’Œ Consulting

đŸ„ 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

‱ Lead CTL activities on studies employing multiple CTLs, coordinating workstreams and supporting delivery to expected quality and timelines ‱ Manage, mentor, train and coach CTL team members and other colleagues, supporting continued career development within the division and ICON ‱ 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 ‱ Create educational materials that effectively communicate the science behind the clinical trial and support consistent site understanding ‱ Build trusted relationships with investigators and site personnel to facilitate effective study conduct and site engagement ‱ Identify scientific and operational barriers affecting recruitment, retention and data quality, and work with study teams to address them ‱ Identify effective pre-screening strategies for each trial and recommend practical improvements based on site feedback and patient pathways ‱ Provide detailed, timely reports of interactions with investigators and site staff, including relevant insights for project teams ‱ Contribute to tools, materials and strategies that support site engagement and performance ‱ Participate in business development activities and represent the CTL function as assigned

🎯 Requirements

‱ Doctoral-degree level qualification such as a PhD, MD or PharmD in a relevant scientific, medical, pharmacy or healthcare discipline ‱ Substantial experience in clinical research, medical affairs or field-based roles involving direct interaction with investigators and clinical trial sites ‱ Strong understanding of clinical trial design, Good Clinical Practice (GCP) and site operations ‱ Ability to interpret complex medical and scientific information and explain protocol concepts clearly to different audiences ‱ Proven relationship-building skills and credibility with clinicians, investigators and site teams ‱ Demonstrated leadership and people-management capability, including experience coaching, mentoring and developing others ‱ Excellent communication, presentation, influencing and problem-solving skills ‱ Ability to manage competing priorities and work effectively in a matrixed, global environment ‱ Legal right to work in the country where the role is based

đŸ–ïž 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

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