iconplc - Hybrid work

Regulatory Affairs Specialist needed in Bogota, Colombia. Join ICON, a world-leading clinical research organization. You will manage regulatory submissions, amendments, and health record maintenance for Colombian authorities. Requires a Pharmaceutical Chemist degree, 1+ year of regulatory experie...

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...

Join ICON plc as a Clinical Study Specialist in Basking Ridge, NJ, supporting global trials across NA, LAM, EU, APAC, and India. Leverage your TMF, CTMS, and SharePoint expertise to organize reports, coordinate meetings, and review study documents. Requires a Bachelor’s degree and 2+ years of ind...

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...

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...

Join ICON as a Medical Data Reviewer in Blue Bell, PA. Leverage your MD, MBBS, or PharmD to ensure clinical trial data accuracy and safety. Collaborate with global teams on medical review, GCP compliance, and safety signal detection. Enjoy competitive benefits including health insurance, retireme...

ICON Strategic Solutions seeks a Study Start-up Manager in Seoul, South Korea to lead clinical trial operations for phase I-IV studies. You will drive site selection, feasibility, and initiation while managing local teams and vendor performance. Ideal candidates possess a science/medical degree, ...

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...

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...

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...

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...

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...