iconplc - IT - Administration

ICON plc seeks a Supplier Performance Monitor in Raleigh, NC, to oversee data quality and compliance for clinical trials. Ideal candidates possess laboratory auditing experience, with in-vitro diagnostics preferred, and relevant degrees plus 3-12 years of experience. This role involves monitoring...

Join ICON as a Site Management Associate I in São Paulo, Brazil. Support clinical trial site monitoring, ensure GCP compliance, and assist with documentation and data tracking. Ideal for candidates with a life sciences degree and strong organizational skills. Enjoy benefits like annual leave, hea...

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 ...