Braziliya
MeksikaMasofaviyTo‘liq stavkaO‘rta darajaSeniorTalab Qilinadigan Til: inglizchaKlinik operatsiyalarManage compliant clinical trial delivery for ICON’s sponsor-dedicated programs. Lead trial execution, performance improvement, and development of clinical operations staff.
Kosta-Rika
Hindiston
KeniyaMeksikaMasofaviyTo‘liq stavkaJuniorO‘rta darajaTalab Qilinadigan Til: inglizchaAssotsiatsiyalangan mutaxassisUmumiySupport planning, documentation, clinical systems, and study close-out for global sponsor-dedicated trials at ICON. Work with study teams, CROs, vendors, and internal departments to coordinate trial activities.
Monitor sponsor-dedicated clinical trials for ICON and coordinate study setup, documentation, compliance, and investigator relationships. Based in São Paulo, Brazil, this remote role supports clinical research operations.
Amerika Qo‘shma Shtatlari
PensilvaniyaMasofaviyTo‘liq stavkaJuniorO‘rta darajaTalab Qilinadigan Til: inglizchaKlinik operatsiyalarLead regulatory submissions and site activation for ICON Strategic Solutions. Support clinical trial start-up and coordinate stakeholder approvals.
MeksikaMasofaviyTo‘liq stavkaJuniorO‘rta darajaTalab Qilinadigan Til: inglizchaAssotsiatsiyalangan mutaxassisUmumiySupport clinical trial planning, coordination, monitoring, and close-out across ICON sponsor-dedicated programs. Contribute to clinical studies advancing new treatments.
MeksikaMasofaviyTo‘liq stavkaJuniorO‘rta darajaTalab Qilinadigan Til: inglizchaKlinik sinovlar bo'yicha yordamchiUmumiySupport ICON’s sponsor-dedicated clinical trials from Mexico by coordinating study records, regulatory submissions, trial materials, and milestone tracking.
Monitor sponsor-dedicated clinical trials across sites in Chile for ICON, a global healthcare research organization. Support protocol adherence, reliable study data, and participant safety throughout each trial.
XitoyGibridTo‘liq stavkaJuniorO‘rta darajaTalab Qilinadigan Til: inglizchaMijozlar bilan ishlashMijozlarga xizmat ko‘rsatish vakiliSupport patient-centred clinical trial delivery for ICON plc in a hybrid Shanghai role. Coordinate client relationships, project milestones, data analysis, and trial operations.
Support CTIS data management, document uploads, and regulatory submissions for ICON plc’s clinical research operations. Coordinate submission activities and stakeholder follow-up to help advance medicines to patients.
PolshaMasofaviyTo‘liq stavkaO‘rta darajaSeniorTalab Qilinadigan Til: inglizchaTalab Qilinadigan Til: polyakchaUmumiyNegotiate clinical trial agreements, amendments, and site budgets with investigator sites across Poland. Support ICON’s international clinical research and healthcare operations through effective contract management.
Lead global regulatory strategy and submissions for ICON plc’s clinical development programmes in Sydney. Advise on health authority engagement, regulatory planning, and cross-functional programme execution.
Lead clinical trial operations, data review, and regulatory compliance for ICON plc, a global clinical research organization. Coordinate cross-functional teams and study deliverables in a remote role based in Buenos Aires.
Lead clinical trial site management for ICON plc in China, supporting protocol compliance, data integrity, and effective study execution. The role covers site oversight and collaboration across Beijing and Shanghai.
Lead site monitoring, compliance, and trial delivery for ICON plc’s sponsor-dedicated clinical research programs in China.
Amerika Qo‘shma Shtatlari
Illinoys
Missuri
Nebraska
Oklaxoma
TexasSenior Clinical Research Associate overseeing orthopedic medical-device trials for ICON Strategic Solutions. The role covers site monitoring, compliance, data integrity, and trial execution across Midwest and Western regions.
Clinical Trial Manager responsible for clinical study delivery in China with ICON plc. The role covers monitoring, enrollment, budgets, risk management, and coordination across study teams.
