This list contains only the countries for which job offers have been published in the selected language (e.g., in the French version, only job offers written in French are displayed, and in the English version, only those in English).
United States , RALEIGH, BLUE BELL, BASKING RIDGE, NJ, CHICAGO, IL, SEATTLE, WA, DALLAS, TX, HOUSTON, TX
Salary
Not provided
iconplc
Expiration Date
Until further notice
Clinical Outcomes Assessment Analyst
Location
United States , CARY, BLUE BELL, INDIANAPOLIS, MIAMI, TAMPA, DALLAS, HOUSTON
Salary
Not provided
iconplc
Expiration Date
Until further notice
Medical Research Associate
Join ICON plc as a Medical Research Associate/Phlebotomist in San Antonio. You will support clinical trial execution, data collection, and analysis in a vital role. The position requires a medical certification and strong organizational skills. This Sunday-Wednesday schedule includes comprehensiv...
Location
United States , San Antonio
Salary
Not provided
iconplc
Expiration Date
Until further notice
Medical Research Associate
Location
United States , San Antonio
Salary
Not provided
iconplc
Expiration Date
Until further notice
Clinical Research Associate II
Join ICON plc as a Clinical Research Associate II in Bratislava. You will monitor clinical trial sites, ensure GCP compliance, and manage data integrity. This role requires 3-6 years of CRA experience, strong site management skills, and 60% travel. We offer competitive health insurance, retiremen...
Location
Slovakia , Bratislava
Salary
Not provided
iconplc
Expiration Date
Until further notice
Feasibility Strategy & Analytics Lead
Lead our clinical trial feasibility strategy in Reading. Develop data-driven country and site plans to optimize patient recruitment and study delivery. Requires 7+ years in clinical research, drug development knowledge, and strong analytical skills. We offer competitive health insurance, retireme...
Location
United Kingdom , Reading
Salary
Not provided
iconplc
Expiration Date
Until further notice
Regulatory Submissions Manager
Lead regulatory submissions and strategy for drug development at a global CRO. This role in Yerevan requires 6+ years of pharma/biotech experience, including CTA/IND/MAA filings. You will provide expert guidance, manage agency interactions, and ensure compliance. We offer competitive benefits inc...