iconplc - United Kingdom

Join ICON plc as a Clinical Research Associate (SSU CRA) in Reading, UK. This sponsor-dedicated role offers reduced travel and a clear path to a standard CRA position. Leverage your SSV, submission, and site management expertise to ensure GCP compliance. Enjoy competitive benefits including healt...

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 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...

Join ICON plc in Reading as a Senior Clinical Supplies Project Manager. Lead clinical supply projects, ensuring timely delivery for global trials. Utilize your 5+ years of supply chain experience to optimize processes and ensure regulatory compliance. Enjoy competitive benefits while shaping the ...

Join ICON plc as a Senior Clinical Research Associate (CRA) in the UK. Oversee clinical trial sites, ensuring protocol adherence, GCP, and data integrity. This role requires 3+ years' CRA experience, strong site management skills, and 60% travel. We offer competitive health insurance, retirement ...