iconplc - IT - Administration

Join ICON plc as a Clinical Research Associate II in Buenos Aires. You will monitor clinical trial sites, ensure protocol/GCP compliance, and contribute to innovative therapies. This role requires 2+ years of CRA experience, strong organizational skills, and 60% travel. We offer competitive healt...

Join ICON plc's clinical research team in Houston as a Medical Research Associate. Support the design and execution of trials, ensuring data accuracy and quality. Requires a medical certification and strong organizational skills. Enjoy competitive benefits including health insurance and retiremen...

Join ICON plc as a Senior Clinical Data Coordinator in Mexico City. Utilize your 5-7 years of experience with RAVE or Veeva to ensure data quality and regulatory compliance. You will develop data management plans, mentor junior staff, and collaborate with cross-functional teams. We offer competit...

Lead regulatory submissions and strategy as a home-based Manager in Seoul. Utilize 6+ years of pharmaceutical regulatory experience to guide drug development from CTA to post-approval. Enjoy competitive benefits including health insurance and global support, driving excellence at a world-leading ...

Join ICON plc as a Clinical Trial Administrator in Mexico City. Support the design and analysis of clinical trials, ensuring protocol compliance and managing essential documentation. This role requires a scientific degree, knowledge of trial processes, and strong organizational skills. We offer c...

Lead clinical research projects from home in Brazil for a global healthcare leader. Utilize your project management expertise to deliver high-quality results on time and within budget. Enjoy competitive benefits including health insurance and retirement planning. Join ICON plc to shape the future...

Seeking a Global Study Manager with 3+ years in clinical trial management, including phase I oncology. You will oversee global study execution, vendor management, and key document development. This remote US role (Eastern/Central time) offers competitive health insurance and retirement benefits a...

Join ICON plc, a global clinical research leader, as a Set Up Specialist. You will coordinate clinical trial setup, ensuring regulatory compliance and efficient study execution. This role requires a life sciences degree and experience in trial setup or site management. The position offers competi...

Join ICON plc as a Senior Clinical Research Associate in Copenhagen. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. Utilize your extensive CRA experience and monitoring expertise, with 60% travel. Enjoy competitive benefits including health ins...

Join ICON plc, a global clinical research leader, as a remote CRA II based in France. Utilize your 24+ months of independent monitoring experience on Phase II/III commercial trials. You will take full ownership of investigator sites, ensuring data integrity and compliance. We offer competitive be...

Join ICON plc as a Clinical Research Associate I/II in São Paulo. Oversee and coordinate clinical trials, ensuring ICH-GCP compliance and data integrity. This sponsor-dedicated role requires a science/medicine degree, excellent English, and 60% travel readiness. Enjoy health insurance, competitiv...

Join the world's largest CRO as a Senior Clinical Research Associate in Montreal. Utilize your 2+ years of on-site monitoring experience and ICH-GCP expertise to conduct clinical trial site visits. This role requires up to 60% travel and offers competitive health insurance and retirement benefits.