10,000+ employees
Founded 1990
đ Pharmaceuticals
đ§Ź Biotechnology
âïž Healthcare Insurance
Pharmaceuticals âą Biotechnology âą Healthcare Insurance
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„ 50 minutes ago
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10,000+ employees
Founded 1990
đ Pharmaceuticals
đ§Ź Biotechnology
âïž Healthcare Insurance
Pharmaceuticals âą Biotechnology âą Healthcare Insurance
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 Oversee talent acquisition and recruitment operations, balancing quality, timelines, and stakeholder expectations âą Acts as the primary point of contact for study teams, developing evidence-based country and site strategies, enrollment scenarios, and protocol optimization recommendations âą Partners cross-functionally (including analytics and recruitment teams) to align feasibility, enrollment planning, and execution strategy throughout the study lifecycle âą Delivers early feasibility insights, including initial enrollment timelines, country footprint, competitive landscape, and key assumptions to inform operational planning âą Continuously refines country footprint, site strategy, and enrollment assumptions as protocols evolve through feasibility and start-up âą Identifies protocol optimization opportunities using real-world data, investigator input, and patient insights âą Supports investigator/site identification, database development, and global site intelligence coordination âą Leads feasibility outreach, analyzes responses, and provides strategic recommendations for country and site selection âą Develops analytics and scenario modeling to optimize site mix, enrollment timelines, diversity goals, and overall study performance âą Partners with cross-functional teams to improve study start-up efficiency and recruitment cycle times âą Owns delivery against defined KPIs and drives continuous improvement through data, innovation, and streamlined processes âą Builds strong stakeholder relationships to enable effective and efficient study execution
âą BS / RN / MS with 7+ years of relevant experience, or PhD / MD with 3+ âą Strong knowledge of drug development, global feasibility, study start-up, and clinical operations âą Experience in clinical research, including trial conduct, GCP, monitoring, and study/project management âą Proven success in a customer-focused environment with ability to meet stakeholder expectations âą Strong verbal and written communication, presentation, and facilitation skills âą Advanced analytical, strategic planning, and problem-solving abilities âą Ability to synthesize insights from multiple data sources into clear recommendations âą Strong consultancy skills, including influencing, negotiation, and conflict resolution âą Ability to manage multiple priorities under tight timelines with high attention to detail âą Comfortable making complex decisions in ambiguous, fast-paced environments âą Experience aligning activities with broader business strategy and objectives âą Experience with multinational clinical trials
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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