iconplc - United Kingdom, Reading

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...

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...

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...

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...