iconplc

Principal Scientist opportunity in Whitesboro, NY, with ICON plc, a global healthcare leader. Seeking an expert with 5+ years of LCMS bench experience, including LCMSMS (Sciex) and large molecule analysis. PhD preferred in Chemistry or Biochemistry. Enjoy competitive benefits, annual leave, and h...

Join a top-rated laboratory team as a Scientist I in Whitesboro, US. You will develop and perform assays on biological samples for pre-clinical and clinical trials, using techniques like biomarker quantification. A Bachelor’s in Biology, Chemistry, or Biotechnology is required, with a focus on GL...

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 (IHCRA) in Bogota, Colombia. Support clinical trial site monitoring, ensuring GCP and regulatory compliance. Ideal for candidates with a Bachelor's in life sciences and clinical research experience. Enjoy competitive benefits including health insurance, re...

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 as a Clinical Research Associate II/Senior CRA in Warsaw or Poznan, Poland. Leverage your 1+ year of CRA experience and ICH-GCP expertise to conduct site monitoring, ensure data integrity, and advance innovative therapies. Enjoy benefits like health insurance, retirement planning, and g...

Join ICON plc as a Site Management Associate I in Buenos Aires, Argentina. Support clinical trial sites by ensuring protocol compliance and GCP adherence. Ideal for candidates with a life sciences degree and strong organizational skills. Enjoy benefits like health insurance, retirement planning, ...

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...