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 Yesterday
đ”đ± Poland â Remote
â° Full Time
đĄ Mid-level
đ Senior
đ« Community Manager
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 Manage investigator portals from study start-up through study close-out and archiving âą Partner with study teams to develop and implement site engagement and communication strategies âą Create, maintain, and publish portal content including news posts, communications, surveys, forms, dashboards, and study resources âą Coordinate portal launches and ongoing portal activities with study teams and external vendors âą Support portal user management and provide business support to stakeholders âą Lead and facilitate meetings with study teams related to portal planning, implementation, and ongoing study conduct âą Monitor portal activity and engagement, identifying opportunities to improve the site experience âą Investigate, track, and resolve portal-related issues, escalating when appropriate âą Contribute to process improvements, training activities, operational documentation, and best practice development âą Support broader site engagement initiatives and technology-related projects as required
âą Degree in Life Sciences, Health Sciences, or equivalent relevant experience âą Experience working within clinical trials or clinical research âą Experience using investigator portals or similar clinical technology platforms that support study sites and investigators âą Strong understanding of clinical trial processes and study conduct âą Excellent organisational and project coordination skills with the ability to manage multiple activities simultaneously âą Strong written and verbal communication skills âą Experience creating communications, newsletters, site-facing content, or engagement materials âą Advanced Microsoft Office skills, including the ability to analyse and present information effectively âą Ability to work successfully within global, cross-functional teams âą Employment contingent upon having the legal right to work in the country where the role is based âą Preferred: experience supporting global or multi-regional clinical trials âą Preferred: experience working directly with study teams, investigators, sites, or clinical technology vendors âą Preferred: experience delivering training, onboarding, or user support âą Preferred: knowledge of site engagement strategies and change management principles âą Additional language skills would be advantageous
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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