iconplc - United Kingdom

Seeking a Senior Clinical Trial Associate in Reading or Cambridge, UK. Leverage your clinical trial support expertise and regulatory knowledge to manage documentation, coordinate meetings, and ensure compliance. Requires a Bachelor's in a scientific field, strong organizational skills, and profic...

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...

ICON is seeking a proactive Talent Sourcing Recruiter in Reading, UK, to build robust pipelines for critical roles in life sciences and healthcare. You will leverage sourcing tools, social media, and networking to identify and engage top candidates. This role requires a Bachelor's degree, strong ...

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...

Senior Clinical Supplies Project Manager sought by ICON plc, a world-leading clinical research organization. This role manages global pharmaceutical supply and CMC activities across all development phases. Ideal candidates bring 3-4 years of clinical supply project management experience. Enjoy fl...

Seeking a detail-oriented **Project Manager, IRT** in **Reading, UK** to lead system activities from award to closeout. Leverage 4+ years of PM experience and clinical research expertise to drive timelines, budgets, and stakeholder communication. Enjoy benefits like annual leave, health insurance...

Join ICON as a Clinical Research Associate II in Reading, UK, and drive late-phase, real-world evidence studies. You will monitor IP and medical device trials, ensuring ICH-GCP compliance and high-quality data delivery. Ideal for experienced CRAs with a life sciences degree, this role offers site...

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...