iconplc - Remote work

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...

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...

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...

Senior Clinical Research Associate sought for global trials in Sydney, Melbourne, Brisbane, or Adelaide. Requires a Pharmacy degree, 4+ years monitoring experience with strong Oncology and Haematology focus, and ICH-GCP expertise. Manage full site lifecycle from initiation to close-out, ensuring ...

Senior Clinical Research Associate sought in Mannheim, Germany, to oversee multi-site trials ensuring GCP and regulatory compliance. Requires an advanced life sciences degree, extensive CRA experience, and 60% travel. Key duties include site monitoring, data integrity, and stakeholder collaborati...

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 I or II in São Paulo, Brazil. This sponsor-dedicated role requires a university degree in science or medicine, ICH-GCP knowledge, and strong English communication skills. You will independently coordinate study setup and monitoring, manage sponsor qu...

Senior CRA role at ICON: design and monitor clinical trials across multiple US locations. Requires 2+ years CRA experience, ICH-GCP expertise, and 60% travel. Responsibilities include site visits, data integrity, and protocol compliance. Benefits: health insurance, retirement planning, and global...