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„ 1 minute ago
đČ North Carolina, Ohio, +2 more states â Remote
đ” $110.5k - $138.2k / year
â° Full Time
đĄ Mid-level
đ Senior
đ» Ghost score 0%
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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 Manage clinical investigator engagement from identification and qualification through enrollment, database lock support, and study closeout âą Serve as a clinical trial scientific ambassador, explaining protocol intent, scientific rationale, and patient eligibility requirements âą Build and sustain strategic relationships with investigators across trials and therapeutic areas âą Co-create tailored recruitment strategies and identify opportunities to reach new patients and accelerate enrollment âą Capture site insights to optimize feasibility, protocol design, and study conduct âą Lead site-level strategy and risk planning for enrollment and data delivery âą Use performance metrics to anticipate issues and maintain progress toward clinical milestones âą Drive inspection readiness across sites âą Collaborate with cross-functional teams and vendors to resolve operational barriers âą Apply knowledge of local treatment paradigms and standards of care to country/site selection and protocol localization âą Oversee and provide quality assurance for vendor monitoring, escalating risks proactively âą Where applicable, lead end-to-end management of Post-Marketing Safety Studies in compliance with local regulations âą Cultivate a portfolio of strategically aligned investigators and support an exceptional investigator experience âą Conduct data-informed site prospecting and prioritization âą Act as a liaison between field teams, vendors, and investigators âą Represent Investigator Engagement with regulatory agencies, ethics committees, and national research organizations where applicable âą Influence the clinical trial ecosystem and align regional initiatives with enterprise-wide clinical development goals
âą Minimum 5 years of experience in clinical research or pharmaceutical industry with experience directly interacting with or working with HCPs and clinical sites âą Minimum 2 years of relevant clinical or therapeutic area experience in Oncology âą Advanced degree in a scientific or clinical field (PharmD, PhD, MD, or MSc preferred) âą Excellent understanding of GCP, clinical development and operations, and trial lifecycle âą Demonstrated understanding of the therapeutic landscape and standards of care, with the ability to apply this knowledge to decision making âą Proven ability to build credibility and influence HCP community through scientific acumen and relationship strength âą Current Oncology experience is required âą Legal right to work in the country where the role is based âą Ability to travel up to 60%
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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