iconplc - Remote work

Join ICON plc as a Senior Clinical Research Associate (CRA) in a remote role based in Blue Bell, US. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. This position requires extensive CRA experience, strong site management skills, and 60% travel. ...

Join ICON plc as a Senior Clinical Research Associate (CRA) in a home-based role in Germany. Oversee clinical trial activities, ensuring protocol adherence, data integrity, and GCP compliance. This role requires extensive CRA experience, strong site management skills, and a willingness to travel ...

Join ICON Plc as a Senior Clinical Research Associate in Mannheim. Oversee clinical trial sites, ensuring protocol adherence, GCP, and data integrity. This role requires extensive CRA experience, strong site management skills, and 60% travel. We offer competitive health insurance, retirement plan...

Join ICON plc as a Senior Clinical Research Associate in Helsinki. Oversee clinical trials, ensuring protocol adherence, data integrity, and GCP compliance. Requires extensive CRA experience, strong site management skills, and 60% travel. Enjoy competitive benefits including health insurance and ...

Join ICON plc's dynamic team in Seoul as a Regulatory Affairs Specialist. You will design clinical trials, interpret medical data, and prepare key submissions (CT/IND, MAA/NA). This role requires 2-3 years of pharmaceutical regulatory experience. We offer competitive health insurance, retirement ...

Seeking an experienced Senior CRA for oncology trials in the Southeast US. This role requires 5+ years of CRA experience with oncology monitoring and 60% travel. You will ensure protocol/GCP compliance, manage sites, and collaborate cross-functionally. We offer competitive health insurance, retir...

Seeking a Senior Clinical Research Associate specializing in Neurovascular trials. This role requires 3+ years of monitoring experience, deep FDA/ICH-GCP knowledge, and strong site management skills. Based in the Central/Midwest U.S., you will ensure data integrity and patient safety at investiga...

Lead medical strategy and innovation in Neurology as a remote Medical Director at ICON. This pivotal role requires an MD with Board Certification and proven CRO/pharma leadership. You will provide expert guidance, ensure regulatory compliance, and shape clinical development. We offer competitive ...

Lead clinical trials remotely as a Clinical Operations Lead at ICON plc. Oversee planning, execution, and delivery of studies, ensuring compliance with timelines and regulations. This role requires a science/medicine degree, therapeutic expertise, and offers competitive health insurance and retir...

Join ICON plc as a Senior Clinical Site Lead, managing key site relationships on the West Coast. Utilize your 8+ years of clinical operations expertise in oncology, neurology, or immunology to drive study conduct and compliance. This role offers competitive benefits and the opportunity to shape t...

Join ICON plc as a Study Start Up Associate II in Mexico City (home-based). Lead clinical trial initiation, ensure regulatory compliance (ICH-GCP), and manage document submissions. Requires 2+ years in clinical research/regulatory affairs. Enjoy health insurance, competitive retirement plans, and...

Join ICON plc as a Senior CRA specializing in Oncology in the Midwest. This role requires 5+ years of CRA experience with oncology monitoring and 60% travel. You will ensure protocol/GCP compliance, manage sites, and collaborate with cross-functional teams. We offer competitive health insurance, ...