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 3 days ago
đČ North Carolina â Remote
â° Full Time
đĄ Mid-level
đ Senior
đ·ââïž Project Manager
đ» Ghost score 10%
Where this job comes from
Posted on ICON plc's careers page â, not through a job board
First seen by Remote Rocketship 3 days ago
Still open on ICON plc's site. Checked 1 hour ago.
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 Lead and coordinate clinical project activities âą Ensure projects are delivered on time, within budget, and to the highest quality standards âą Coordinate project and programme management delivery âą Resolve project issues and develop team capability âą Define and maintain project or programme scope, plans, timelines, resources and deliverables âą Lead multidisciplinary teams and coordinate functional activities to achieve contractual and operational milestones âą Monitor quality, budget, forecast, risks, issues and dependencies and drive timely corrective action âą Maintain clear governance and communication with clients, sponsors and internal stakeholders âą Ensure delivery follows applicable ICON procedures, ICH GCP requirements and relevant regulations âą Capture lessons learned and implement improvements that strengthen delivery predictability and client outcomes
âą Bachelor's degree in life sciences, healthcare, business or a related discipline, or equivalent relevant experience âą Experience leading complex clinical research projects across multidisciplinary and geographically distributed teams âą Knowledge of clinical trial delivery, ICH Good Clinical Practice (GCP) principles and applicable regulatory requirements âą Experience managing project scope, timelines, resources, risks and financial or budget related activities âą Experience leading multidisciplinary teams and coordinating functional activities to achieve contractual and operational milestones âą Experience monitoring quality, budget, forecast, risks, issues and dependencies and driving timely corrective action âą Experience maintaining clear governance and communication with clients, sponsors and internal stakeholders âą Experience in Obesity, GI, Hepatology, or Dermatology highly preferred âą Proficiency in project management tools and methodologies âą Project management certification such as PMP or PRINCE2 preferred âą Advanced degree in a relevant scientific, healthcare or business discipline preferred âą Experience leading global or multi region clinical studies in a CRO or sponsor environment preferred âą Willingness to travel as required (approximately 30%) âą Legal right to work in the country where the role is based
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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