iconplc - Research and Development

Join ICON plc as a Site Management Associate I in Buenos Aires, Argentina. Support clinical trial sites by ensuring protocol compliance and GCP adherence. Ideal for candidates with a life sciences degree and strong organizational skills. Enjoy benefits like health insurance, retirement planning, ...

Senior Clinical Research Associate sought for global trials in Sydney, Melbourne, Brisbane, or Adelaide. Requires a Pharmacy degree, 4+ years monitoring experience with strong Oncology and Haematology focus, and ICH-GCP expertise. Manage full site lifecycle from initiation to close-out, ensuring ...

Join ICON plc as a Clinical Research Associate I or II in São Paulo, Brazil. This sponsor-dedicated role requires a university degree in science or medicine, ICH-GCP knowledge, and strong English communication skills. You will independently coordinate study setup and monitoring, manage sponsor qu...

Senior CRA role at ICON: design and monitor clinical trials across multiple US locations. Requires 2+ years CRA experience, ICH-GCP expertise, and 60% travel. Responsibilities include site visits, data integrity, and protocol compliance. Benefits: health insurance, retirement planning, and global...

Join AstraZeneca Canada as a Clinical Trial Associate in Burlington, ON. Leverage your oncology experience and clinical research expertise to coordinate trials, manage regulatory documentation, and support cross-functional teams. This hybrid role requires a Bachelor’s in a scientific field and st...

Join ICON as a Clinical Research Associate II in Seoul, South Korea. Leverage 2+ years of CRA experience and ICH-GCP expertise to conduct site monitoring, ensure data integrity, and advance innovative therapies. Enjoy comprehensive benefits including health insurance, retirement planning, and glo...

Join ICON, a world-leading clinical research organization, as a Contract Senior Clinical Research Associate in Los Angeles. This 6-month role requires 3+ years of independent monitoring, ICH-GCP expertise, and 80% travel. You will oversee site visits, ensure protocol compliance, and drive data in...

Lead clinical trial oversight and site management as a Senior CRA with ICON Plc in Singapore. Utilize your extensive monitoring expertise to ensure protocol adherence, data integrity, and GCP compliance across multiple sites. This role offers competitive benefits and requires approximately 60% tr...