iconplc - Remote work

Join ICON plc as a Senior Clinical Research Associate in Frankfurt. 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...

Join ICON plc as a Senior Clinical Research Associate in Oslo. Oversee clinical trials, ensure ICH-GCP compliance, and analyze data. Requires fluency in Norwegian and English, plus 60% travel. Enjoy health insurance, competitive retirement plans, and a global support program.

Seeking an experienced Senior Clinical Research Associate (CRA) for oncology trials in the Midwest. You will monitor sites, ensure GCP compliance, and manage stakeholder relationships. This role offers competitive benefits including health insurance and requires extensive CRA experience with onco...

Join ICON plc as a Clinical Research Associate II in Dublin, Ireland. 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 p...

Join ICON plc as a Clinical Research Associate II in a remote role based in Colombia. 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 insuran...

Lead early-phase oncology trials as a Clinical Trial Manager at ICON in Raleigh or Blue Bell. Utilize your 5+ years of experience, including oncology and multinational trial management, to drive study success. This role offers competitive benefits and focuses on vendor oversight and regulatory co...

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...