iconplc - Remote work

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.

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...

Join ICON plc as a Clinical Research Associate in the United States. You will monitor clinical trial sites, ensure ICH-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 Clinical Research Associate in Ophthalmology. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and patient safety across multiple sites. This role requires extensive CRA experience, expertise in GCP, and 60% travel. We offer competitive hea...