iconplc - Remote work

Join ICON plc in Seoul as a Study Start Up Associate I and help shape the future of clinical development. You will facilitate clinical trial initiation, ensure regulatory compliance, and prepare key submissions like INDs. This role requires a life sciences degree, strong organizational skills, an...

Lead global clinical trials from Seoul with ICON, a top CRO. Utilize your 10+ years of trial management expertise to oversee budgets, drive enrollment, and mentor CRAs. This senior role offers competitive health insurance, retirement planning, and a chance to shape the future of clinical developm...

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...

Senior CTA opportunity at ICON in the United States. Ensure clinical trial site compliance with GCP and regulatory standards. Requires a Bachelor’s in life sciences or clinical research, plus strong site management and analytical skills. Benefits include health insurance, retirement plans, life a...

Join ICON plc as a Contracts Lead Investigator in Mexico City. You will review, negotiate, and manage clinical trial and vendor contracts, ensuring regulatory compliance. The role requires 2+ years of contract management experience, preferably in pharma or clinical research. We offer competitive ...

Join ICON plc as a Site Management Associate II with French in Warsaw. Support clinical trial site management, ensuring GCP compliance and protocol adherence. Requires a Bachelor’s in life sciences, clinical research experience, and fluency in English and French. Enjoy benefits like annual leave,...

Join ICON plc as a Clinical Research Associate II in the United States. You will monitor clinical trial sites, ensure protocol/GCP compliance, and contribute to advancing innovative therapies. This role requires 2+ years of CRA experience, ICH-GCP knowledge, and 60% travel. We offer competitive h...

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...

Join ICON plc as a Senior Clinical Research Associate (CRA) in a home-based role in France. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and regulatory compliance. This role requires extensive CRA experience, Phase I Oncology expertise, and 60% travel. We offer ...