iconplc - IT - Administration

Join ICON plc as a Senior Clinical Research Associate in Oncology. Oversee clinical trials on the US West Coast, ensuring protocol compliance and data integrity. This role requires 5+ years of CRA experience with oncology monitoring and 60% travel. We offer competitive health insurance, retiremen...

Join ICON plc as a Senior Clinical Research Associate in Bangkok. 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, ...

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

Join ICON plc in Bangkok as a Clinical Research Associate II. Utilize your 2+ years of CRA experience and ICH-GCP knowledge to monitor sites and ensure data integrity. This role involves 60% travel to advance clinical trials in a dynamic, global environment. We offer competitive health insurance ...

Join ICON plc as a Clinical Research Associate II in a fully remote, FSP model role based in Frankfurt. You will monitor clinical trial sites, ensure ICH-GCP compliance, and contribute to advancing innovative therapies. This role requires 2+ years of CRA experience, strong organizational skills, ...

Join ICON in Shanghai as a Site Specialist II, a key role in clinical trial execution. You will conduct site visits, ensure protocol/GCP compliance, and manage data integrity. Requires a Bachelor's degree, 3+ years of SSU experience, and strong organizational skills. We offer competitive benefits...

Lead pharmacovigilance activities for a global CRO in Sao Paulo, Brazil. Oversee drug safety monitoring, adverse event reporting, and ensure regulatory compliance. This senior role requires significant PV experience, strong leadership, and a life sciences degree. We offer competitive health insur...

Join ICON plc as a Clinical Research Associate II in Hangzhou. 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 health in...

Join ICON plc as a Clinical Research Associate II in Barcelona or Madrid. You will monitor clinical trial sites, ensure protocol/GCP compliance, and contribute to advancing treatments. This role requires 2+ years of CRA experience, strong organizational skills, and 60% travel. We offer competitiv...

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

Join ICON plc as a Senior CRA/CRA II in Belém do Pará. Design and analyze clinical trials, ensuring protocol compliance and data integrity. We require a Bachelor's degree, solid CRA experience, and ICH-GCP knowledge. Enjoy competitive benefits including health insurance and flexible offerings.

Join ICON plc as a Senior Clinical Research Associate or CRA II in the United States. You will design and analyze clinical trials, ensuring protocol compliance and data integrity. This role requires 1-3+ years of independent monitoring experience, ICH-GCP knowledge, and 60% travel. We offer compe...