iconplc - United Kingdom, Research and Development

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...

Join ICON plc as a Senior Clinical Research Associate (CRA) in the UK. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. This role requires extensive CRA experience, site management expertise, and domestic travel. We offer competitive benefits inc...

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, a global clinical research leader, as a Clinical Site Associate in Reading, UK. Support trial operations by ensuring site compliance, documentation accuracy, and audit readiness. This role requires a life sciences degree, strong organizational skills, and offers competitive benefit...