iconplc - United Kingdom, Remote work

Lead clinical trials as Director, Clinical Operations at ICON in Sofia, Warsaw, Belfast, Poland, or Ireland. Drive performance, ensure GCP compliance, and manage cross-functional teams to advance innovative therapies. Requires a life sciences degree and extensive CRO/pharma experience. Enjoy comp...

Join ICON as a UK home-based Clinical Research Associate 1, specializing in In Vitro Diagnostics. This unique role offers a transition from lab-based work into clinical trial operations on a blue-chip diagnostics project. You will coordinate study initiation, monitoring, and completion while ensu...

Join ICON as a home-based Clinical Research Associate in the UK. Leverage your ICH-GCP expertise and monitoring experience to oversee clinical trials, ensuring patient safety and data quality. This role requires a science degree, UK driving licence, and 40% travel to hospital sites. Enjoy flexibl...

Lead innovative training development at ICON in Belfast, UK. This role designs cutting-edge learning solutions for clinical research, pharmacovigilance, and regulatory teams. Requires 5+ years in learning design, expertise in Articulate 360 and Vyond, and strong project management skills. Enjoy b...

Join ICON plc as a Global Study Manager in Reading, UK. Lead the design and analysis of global clinical trials, ensuring regulatory compliance. Utilize your 5+ years of trial management expertise to advance innovative therapies. We offer competitive benefits including health insurance and a suppo...

Lead patient recruitment strategies for clinical trials at ICON plc in Reading. Utilize your 7+ years of experience in clinical research and digital marketing to enhance patient access and engagement. You will analyze metrics, lead cross-functional teams, and build key partnerships. We offer comp...

Lead our clinical trial feasibility strategy in Reading. Develop data-driven country and site plans to optimize patient recruitment and study delivery. Requires 7+ years in clinical research, drug development knowledge, and strong analytical skills. We offer competitive health insurance, retireme...

Join ICON plc as a Clinical Research Associate II in Reading. You will conduct site monitoring visits, ensure ICH-GCP compliance, and contribute to innovative clinical trials. This role requires 2+ years of CRA experience, strong organizational skills, and 60% travel. We offer competitive benefit...