iconplc

Lead global clinical trials from Mexico City as a Senior Clinical Trial Manager with ICON. Utilize your 7+ years of CTM experience, including expertise in North America and LATAM studies, to oversee budgets, drive enrollment, and ensure study integrity. Enjoy competitive benefits while shaping th...

Join our team in Mexico City as a Regulatory Technician. You will manage clinical trial submissions using the CTIS system, ensuring compliance and quality. Ideal candidates have advanced English and 1-2 years in clinical research. We offer competitive health insurance and retirement plans.

Join ICON plc as a Senior CRA or CRA in Blue Bell, USA. You will ensure protocol compliance and data integrity across clinical trial sites, requiring 1-3+ years of monitoring experience and ICH-GCP knowledge. This role involves ~60% travel and offers competitive health insurance, retirement plans...

Join ICON plc, a global clinical research leader, as a Senior CRA or CRA II in Blue Bell. Utilize your monitoring experience and ICH-GCP knowledge to ensure trial integrity and patient safety. This role offers significant travel, competitive benefits, and a chance to shape the future of healthcare.

Join ICON plc as a Medical Research Associate in San Antonio. Support clinical trial design, execution, and data management, ensuring accuracy and quality. Requires a medical certification and strong organizational skills. Enjoy competitive benefits including health insurance and retirement plann...

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, 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...