iconplc

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...

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...

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...

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...

ICON seeks a Clinical Trial Liaison (CTL) in Phoenix, AZ, to drive site engagement and patient enrollment. This field-based role requires a doctoral degree (M.D., PharmD, PhD) and expertise in cardiometabolic, neuroscience, or oncology. You will provide scientific support, optimize recruitment st...

ICON plc seeks a Medical Research Associate (Phlebotomist) for a Fri-Sun day shift in San Antonio, TX. Join a world-leading clinical research organization to support clinical trials, data collection, and regulatory compliance. Ideal for Medical Assistants, Phlebotomy Technicians, or LVNs with str...

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...