iconplc - United Kingdom, Remote work

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...

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 ...

Join a global pharmaceutical leader as a Site Investigational Product Specialist in Reading, UK. Utilize your extensive clinical trial and IP administration expertise (IV, SC, IM) in Oncology/Immunology. Ensure safe investigational product preparation and serve as the key liaison between sponsor ...

Join ICON plc as a Senior Clinical Research Associate in Reading, UK. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. This role requires extensive CRA experience, strong site management skills, and 60% travel. We offer competitive health insuran...

Join the world's largest CRO as a Clinical Data Engineer in Livingston. Design and implement enterprise-level data pipelines for clinical trial integration using Python, SQL, and cloud platforms (AWS/Azure). Leverage 8+ years of experience to ensure high-quality data delivery for regulatory compl...