iconplc - IT - Administration

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 Contract Analyst II in Beijing or Shanghai. Leverage your 2+ years of contract administration experience and legal expertise to review, negotiate, and manage clinical trial agreements. Collaborate with cross-functional teams to ensure regulatory compliance and mitigate risks. E...

ICON plc seeks a Clinical Trial Liaison in Sofia, Bulgaria. This field-based role provides scientific support to investigators, driving patient enrollment and study success. Ideal candidates hold a PhD, PharmD, or MD with clinical research experience. Enjoy competitive benefits including health i...

Global Study Manager opportunity in Barcelona with ICON Strategic Solutions, embedded within a leading biopharmaceutical FSP team. You will oversee global clinical studies, manage vendors, and ensure ICH-GCP compliance. Requires 5+ years clinical research experience, 3+ in global project manageme...

Join ICON Plc as a Clinical Research Associate (CRA) in Oncology across multiple US locations. Leverage your advanced life sciences degree and extensive CRA experience to oversee trial sites, ensure GCP compliance, and manage data integrity. This role demands 60% travel and strong site management...

Join ICON plc as a Clinical Research Associate II in Paris, France. This FSP role offers hybrid or home-based flexibility with a top-tier global pharmaceutical partner. You will independently monitor Phase II–IV trials across Neurology, Rare Disease, Dermatology, and Oncology. Requires 2-3 years ...

Senior Clinical Research Associate sought for ICON’s FSP division in Paris. This hybrid or home-based role offers a productivity bonus and excellent benefits while managing Phase II–IV trials for a top French pharmaceutical leader. Requires fluency in French, 4+ years of independent monitoring, a...

Join ICON Strategic Solutions as a Drug Safety Associate in a home-based role in South Korea. Leverage your pharmacovigilance expertise to manage adverse event reporting, safety data entry, and regulatory submissions. Ideal for candidates with 1+ year experience, a life science or healthcare degr...

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...

Senior Clinical Research Associate sought by ICON Plc in Madrid to lead site monitoring and trial management. This role demands expertise in GCP, regulatory compliance, and data integrity, with 60% travel. Ideal candidates possess a scientific degree, strong organizational skills, and experience ...

ICON seeks a Project Coordinator II in Blue Bell, PA, to drive project success through meticulous schedule management, documentation, and cross-functional communication. Ideal candidates possess a Bachelor’s degree or relevant experience, strong organizational skills, and proficiency in Microsoft...