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Join ICON plc as a Clinical Research Associate in São Paulo. Oversee and coordinate clinical trials, ensuring ICH-GCP compliance and data integrity. This role requires a science/medicine degree, excellent English, and 60% travel readiness. We offer health insurance, competitive retirement plans, ...

Join ICON plc as a Clinical Research Associate II in São Paulo. You will design trials, analyze complex medical data, and ensure protocol compliance with ICH-GCP. This role requires a scientific degree, on-site monitoring experience, and 60% travel. We offer competitive health insurance and retir...

Join ICON plc as a Clinical Research Associate II in São Paulo. You will monitor clinical trial sites, ensure protocol/GCP compliance, and contribute to advancing new therapies. This role requires a science degree, CRA experience, and 60% travel. We offer competitive health insurance, retirement ...

Join ICON plc as a Clinical Research Associate II in São Paulo. You will monitor clinical trial sites, ensure ICH-GCP compliance, and contribute to advancing treatments. The role requires a scientific degree, CRA experience, and 60% travel. We offer competitive health insurance and retirement plans.

Join ICON plc, a global clinical research leader, as a Clinical Research Associate in Reading, UK. You will manage phase I-IV trial sites, ensuring GCP compliance and successful study delivery. This role requires monitoring experience and offers competitive benefits with significant travel.

Join ICON plc as a Senior Clinical Research Associate in Taipei. 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 insurance, r...

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 ICON plc as a Freelance Senior CRA in Prague. Oversee clinical trial sites, ensuring protocol adherence, GCP, and data integrity. Requires fluency in English & Czech, extensive CRA experience, and 60% travel. Enjoy competitive benefits including health insurance and a global support program.

Join ICON plc as a Senior Medical Writer and shape the future of clinical development. Lead medical writing strategies for key clinical documents like protocols and CSRs. Utilize your 3-5+ years of CRO/pharma experience and regulatory knowledge in a dynamic, global team. Enjoy competitive benefit...

Join ICON plc as an Investigator Payment Associate in São Paulo. You will ensure accurate, compliant financial processing for global clinical trials. This role requires a finance/accounting background and knowledge of regulations like the Sunshine Act. We offer competitive health insurance, retir...

Join ICON plc as a Clinical Research Lead Assistant and help shape the future of clinical development. This remote role requires strong organizational skills, fluency in English, and proficiency in Microsoft applications to provide key administrative support for clinical trials. We offer competit...

Lead global clinical trials from start-up to database lock as a Senior Clinical Trial Manager at ICON in Boston. Utilize your 10+ years of experience to oversee budgets, drive enrollment, and mentor CRAs. This pivotal role offers competitive health insurance, retirement planning, and a chance to ...