iconplc - Remote work

Join ICON plc as a Senior Clinical Research Associate in Athens, Greece. Oversee oncology clinical trials, ensuring protocol adherence, data integrity, and GCP compliance. This role requires 12+ months of monitoring experience and offers extensive travel, competitive benefits, and a chance to sha...

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, ...

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 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...

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 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, a global clinical research leader, as a Senior Clinical Research Associate in Romania. This remote, client-dedicated role involves monitoring Phase I-IV trials across therapeutic areas, requiring 3.5+ years of independent monitoring experience and 60% travel. We offer competitive b...

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 Clinical Research Associate II in Sao Paulo. 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 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.