iconplc

Lead bioanalytical laboratory operations at ICON in Whitesboro, NY. Oversee a team, manage workflows, and ensure GLP compliance to deliver high-quality data for clinical trials. Requires a relevant degree, lab management experience, and strong leadership skills. We offer competitive health insura...

Join ICON plc as a Scientist I in Whitesboro, NY. You will develop and perform assays for clinical trials, ensuring compliance with GLP/GCP standards. The role requires a Bachelor's in Biology or related field and experience with binding assays. We offer a competitive salary, annual bonus, and co...

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...

Seeking a Senior Clinical Site Manager (CRA) for a part-time, home-based role in Melbourne or Sydney. This position requires extensive monitoring experience, GCP knowledge, and 50% travel. You will ensure protocol compliance and drive site performance for a leading pharmaceutical client. We offer...

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, a global clinical research leader, as a Clinical Site Associate in Bangkok. You will ensure site compliance, manage documentation, and support audit readiness for clinical trials. This role requires a life sciences degree, strong organizational skills, and fluency in English. Enjoy...

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 as a Senior Pharmacovigilance Associate in a 100% remote role based in Brazil. Utilize your extensive drug safety experience to manage adverse event reporting, signal detection, and regulatory submissions. This key position offers competitive benefits while ensuring patient safety and c...

Lead pharmacovigilance operations in Brazil for ICON plc, a global healthcare intelligence leader. Supervise safety monitoring, adverse event reporting, and ensure regulatory compliance for clinical trials. This role requires a life sciences degree, PV experience, and strong leadership skills. We...

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 Site Associate in Kuala Lumpur. Support global clinical trials, managing site communications, TMF/ISF documents, and ensuring GCP compliance. Requires a life sciences degree and strong organizational skills. Enjoy health insurance, competitive retirement plans, and a s...