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Clinical Trial Liaison

đŸ”„ 1 minute ago

đŸŒČ North Carolina, Ohio, +2 more states – Remote

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đŸ’” $110.5k - $138.2k / year

⏰ Full Time

🟡 Mid-level

🟠 Senior

đŸ‘» Ghost score 0%

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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

‱ Manage clinical investigator engagement from identification and qualification through enrollment, database lock support, and study closeout ‱ Serve as a clinical trial scientific ambassador, explaining protocol intent, scientific rationale, and patient eligibility requirements ‱ Build and sustain strategic relationships with investigators across trials and therapeutic areas ‱ Co-create tailored recruitment strategies and identify opportunities to reach new patients and accelerate enrollment ‱ Capture site insights to optimize feasibility, protocol design, and study conduct ‱ Lead site-level strategy and risk planning for enrollment and data delivery ‱ Use performance metrics to anticipate issues and maintain progress toward clinical milestones ‱ Drive inspection readiness across sites ‱ Collaborate with cross-functional teams and vendors to resolve operational barriers ‱ Apply knowledge of local treatment paradigms and standards of care to country/site selection and protocol localization ‱ Oversee and provide quality assurance for vendor monitoring, escalating risks proactively ‱ Where applicable, lead end-to-end management of Post-Marketing Safety Studies in compliance with local regulations ‱ Cultivate a portfolio of strategically aligned investigators and support an exceptional investigator experience ‱ Conduct data-informed site prospecting and prioritization ‱ Act as a liaison between field teams, vendors, and investigators ‱ Represent Investigator Engagement with regulatory agencies, ethics committees, and national research organizations where applicable ‱ Influence the clinical trial ecosystem and align regional initiatives with enterprise-wide clinical development goals

🎯 Requirements

‱ Minimum 5 years of experience in clinical research or pharmaceutical industry with experience directly interacting with or working with HCPs and clinical sites ‱ Minimum 2 years of relevant clinical or therapeutic area experience in Oncology ‱ Advanced degree in a scientific or clinical field (PharmD, PhD, MD, or MSc preferred) ‱ Excellent understanding of GCP, clinical development and operations, and trial lifecycle ‱ Demonstrated understanding of the therapeutic landscape and standards of care, with the ability to apply this knowledge to decision making ‱ Proven ability to build credibility and influence HCP community through scientific acumen and relationship strength ‱ Current Oncology experience is required ‱ Legal right to work in the country where the role is based ‱ Ability to travel up to 60%

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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