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).
Join ICON as a Site Management Associate II in Buenos Aires, Argentina. Leverage 3+ years of clinical trial administration experience to lead TMF and eISF oversight, mentor new CTAs, and ensure GCP compliance. This role offers leadership development, health insurance, and retirement planning. Adv...
Location
Argentina , Buenos Aires
Salary
Not provided
iconplc
Expiration Date
Until further notice
Clinical Study Specialist
Location
United States , Basking Ridge
Salary
Not provided
iconplc
Expiration Date
Until further notice
Clinical Study Specialist
Clinical Study Specialist role at ICON plc, a global leader in clinical research. Based in Warren NJ, Armonk NY, or Cambridge MA (hybrid). Requires a Bachelor’s degree and 2+ years industry experience supporting global trials with TMF, CTMS, and SharePoint. Enjoy competitive benefits, annual leav...
Location
United States , Boston; Basking Ridge, NJ
Salary
Not provided
iconplc
Expiration Date
Until further notice
Clinical Trial Associate
Join AstraZeneca Canada as a Clinical Trial Associate in Burlington, ON. Leverage your oncology experience and clinical research expertise to coordinate trials, manage regulatory documentation, and support cross-functional teams. This hybrid role requires a Bachelor’s in a scientific field and st...
Location
Canada , Burlington
Salary
50648.00 - 63310.00 CAD / Year
iconplc
Expiration Date
Until further notice
Medical Data Reviewer
Location
United States , Blue Bell
Salary
Not provided
iconplc
Expiration Date
Until further notice
Study Start-up Manager-South Korea-ICON Strategic Solutions
Location
South Korea , Seoul
Salary
Not provided
iconplc
Expiration Date
Until further notice
Senior Clinical Research Associate
Senior Clinical Research Associate (CRA II) sought for a hybrid role in Bucharest, Romania, specializing in oncology. You will independently monitor clinical trials, ensuring GCP and regulatory compliance across SSVs, SIVs, IMVs, and COVs. Requires 18+ months of on-site monitoring experience, a l...
Location
Romania , Bucharest
Salary
Not provided
iconplc
Expiration Date
Until further notice
Global Logistics Associate
Global Logistics Associate sought by ICON plc, a leading clinical research organization, to manage global supply chain operations from Mexico City. This role requires a Bachelor’s degree and 3+ years of logistics experience in clinical trials or pharmaceuticals. You will coordinate study-specific...
Location
Mexico , Mexico City
Salary
Not provided
iconplc
Expiration Date
Until further notice
Global Logistics Associate
Global Logistics Associate role in Warsaw, Poland, coordinating global supply chain operations for ICON. Requires a Bachelor’s degree and 1-2 years of logistics experience, ideally in pharma or CRO. Key duties include managing international shipments, optimizing logistics strategies, and maintain...
Location
Poland , Warsaw
Salary
Not provided
iconplc
Expiration Date
Until further notice
Clinical Research Associate II
Join ICON as a Clinical Research Associate II in Seoul, South Korea. Leverage 2+ years of CRA experience and ICH-GCP expertise to design and monitor clinical trials, ensuring data integrity and patient safety. Enjoy extensive travel (60%), competitive benefits, and global support. Advance innovat...
Location
South Korea , Seoul
Salary
Not provided
iconplc
Expiration Date
Until further notice
Talent Sourcing Recruiter
ICON plc seeks a Talent Sourcing Recruiter in Raleigh, NC, to build robust pipelines for critical roles in clinical research. You will proactively identify and engage candidates using sourcing tools, social media, and networking. Ideal candidates have recruiting experience in life sciences or hea...
Location
United States , Raleigh
Salary
Not provided
iconplc
Expiration Date
Until further notice
Clinical Research Associate II
ICON seeks a Clinical Research Associate II in Hangzhou, China, to design and analyze clinical trials. You will ensure protocol compliance, data integrity, and patient safety while conducting site visits. Requires a Bachelor’s degree, 2+ years of CRA experience, and ICH-GCP knowledge. Benefits in...