Amerika Qo‘shma ShtatlariMasofaviyTo‘liq stavkaJuniorO‘rta darajaTalab Qilinadigan Til: inglizchaKlinik tadqiqotLead clinical data management delivery for EDETEK’s CONFORM eClinical implementations and clinical trial projects. Oversee client coordination, user acceptance testing, documentation, and development of junior team members.
Amerika Qo‘shma Shtatlari
PensilvaniyaCoordinate participant recruitment, study visits, regulatory submissions, and data management for clinical research at the University of Pennsylvania. Support clinical investigations at Penn’s Perelman School of Medicine.
XitoyMasofaviyTo‘liq stavkaJuniorO‘rta darajaDiplom talab qilinmaydiTalab Qilinadigan Til: inglizchaKlinik tadqiqotSupport AbbVie oncology trials in China by monitoring clinical sites, managing study risks and helping protect compliance, recruitment and data quality.
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 ShtatlariPensilvaniyaCoordinate participant visits, informed consent, data collection, and IRB compliance for University of Pennsylvania clinical studies. Support research activities at study sites in Philadelphia.
Amerika Qo‘shma ShtatlariLead early-phase clinical research advancing medicines for Alzheimer’s, Parkinson’s, ALS, and other neurodegenerative diseases. Shape trial design, analyze evidence, and support regulatory development.
Amerika Qo‘shma Shtatlari
Kaliforniya
Kolorado
MinnesotaOversee clinical sites, study documentation, and data quality for Medtronic neurovascular device studies. Coordinate compliant study delivery with investigators, vendors, monitors, and internal teams.
Amerika Qo‘shma Shtatlari
Merilend
VirjiniyaMasofaviyTo‘liq stavkaJuniorO‘rta darajaDiplom talab qilinmaydiTalab Qilinadigan Til: inglizchaKlinik tadqiqotMonitor oncology clinical trial sites for Parexel, a provider of clinical development, regulatory, consulting, and market access services. Oversee site compliance, participant safety and recruitment, and study documentation.
Amerika Qo‘shma Shtatlari
ArizonaMasofaviyTo‘liq stavkaJuniorO‘rta darajaTalab Qilinadigan Til: inglizchaKlinik tadqiqotOversee investigator sites and monitor clinical trials for Parexel, supporting patient safety, GCP compliance, recruitment, and study quality. The role covers sites across the United States and is listed as remote in Arizona.
Amerika Qo‘shma ShtatlariKaliforniyaKoloradoMinnesotaOversee clinical study sites, data quality, and regulatory records for Medtronic’s neurovascular technologies. Support compliant studies from site activation through closeout.
Amerika Qo‘shma ShtatlariKaliforniyaSupport AbbVie’s neurology clinical trials by monitoring research sites and helping uphold regulatory compliance, data quality, patient safety, and recruitment goals.
Amerika Qo‘shma ShtatlariPensilvaniyaCoordinate participant screening, study visits, data collection, and regulatory tasks for clinical research at the University of Pennsylvania Perelman School of Medicine.
Amerika Qo‘shma ShtatlariPensilvaniyaCoordinate participant visits, study protocols, IRB submissions, and clinical data for the University of Pennsylvania’s medical research programs.
Amerika Qo‘shma Shtatlari
ViskonsinAnalyze industry-sponsored clinical trial data for UW–Madison’s Statistical Data Analysis Center. Support independent data monitoring committees with statistical methods, study design, and reporting.
Amerika Qo‘shma Shtatlari
Nyu-JersiLead a team of clinical research associates overseeing neurology trial monitoring, site performance, and compliant study delivery at MSD. The role also covers team development, resource planning, and coordination with clinical and operational partners.
Amerika Qo‘shma Shtatlari
IllinoysMasofaviyTo‘liq stavkaSeniorTalab Qilinadigan Til: inglizchaKlinik tadqiqotOversee investigator sites and clinical trial monitoring for Parexel across the Central or Western United States. Support patient safety, GCP compliance, recruitment, and study quality throughout the trial lifecycle.
