iconplc - Remote work

Join ICON plc, a global clinical research leader, as a Senior Contract Analyst in Blue Bell, US. You will manage and negotiate clinical trial contracts, ensuring compliance and mitigating risks. The role requires a business/legal degree, industry experience, and strong analytical skills. We offer...

Lead complex clinical trial programs as a Trial Delivery Lead at ICON in Blue Bell. Utilize your extensive program management expertise to deliver large-scale projects on time and within budget. This role offers competitive benefits and requires strong leadership to guide cross-functional teams.

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

Join ICON plc as a Senior Clinical Research Associate in a remote role based in France. You will design and analyze clinical trials, ensuring protocol compliance and data integrity. This position requires 2+ years of CRA experience, ICH-GCP knowledge, and 60% travel. We offer competitive health i...

Join ICON plc in Milan as a Clinical Research Associate II. You will design and analyze clinical trials, ensuring protocol compliance and data integrity. This role requires 2+ years of CRA experience, ICH-GCP knowledge, and 60% travel. We offer competitive health insurance, retirement planning, a...

Join ICON plc as a Clinical Research Associate II in Prague. 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 insu...

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

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

Join ICON plc, a global clinical research leader, as a Clinical Trial Associate. This role focuses on study start-up support and vendor management within the US. We seek organized professionals with CRO/pharma experience and strong communication skills. Enjoy competitive benefits including health...

Lead regional clinical trial operations for a global CRO. This Boston or Philadelphia-based role requires 5-7 years' experience, including 3+ years in trial execution and direct team management. Oncology/hematology expertise is preferred. We offer a competitive salary, comprehensive benefits, and...

Seeking an Associate Director of Regional Clinical Operations to oversee clinical trials in the Southern US (Atlanta, Houston, Tampa, Dallas). This role requires 5-7 years in clinical operations, including 3+ years in trial execution and direct team management. Ideal candidates have global trial ...

Join ICON plc as a Site Activation and Maintenance Associate I in Raleigh or Blue Bell. You will manage 25-30 sites, handling regulatory documents, IRB communication, and compliance. This role requires a Bachelor's degree and clinical research experience. We offer competitive health insurance, re...