Statele Unite ale Americii
ArizonaRemoteNormă întreagăJuniorNivel mediuLimbă Obligatorie: englezăCercetare clinicăOversee 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.
Statele Unite ale Americii
California
Colorado
MinnesotaOversee clinical study sites, data quality, and regulatory records for Medtronic’s neurovascular technologies. Support compliant studies from site activation through closeout.
Statele Unite ale AmericiiCaliforniaSupport AbbVie’s neurology clinical trials by monitoring research sites and helping uphold regulatory compliance, data quality, patient safety, and recruitment goals.
Statele Unite ale Americii
PennsylvaniaCoordinate participant screening, study visits, data collection, and regulatory tasks for clinical research at the University of Pennsylvania Perelman School of Medicine.
Statele Unite ale AmericiiPennsylvaniaCoordinate participant visits, study protocols, IRB submissions, and clinical data for the University of Pennsylvania’s medical research programs.
MexicRemoteNormă întreagăJuniorNivel mediuLimbă Obligatorie: englezăAsociat pentru studii cliniceGeneralSupport ICON’s sponsor-dedicated clinical trials from Mexico by coordinating study records, regulatory submissions, trial materials, and milestone tracking.
Statele Unite ale Americii
WisconsinAnalyze 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.
Statele Unite ale Americii
New Jersey
New YorkSupport clinical trial operations at Regeneron, a medicines developer, by tracking study progress, documentation, sites, vendors, and close-out work.
Statele Unite ale AmericiiNew JerseyLead 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.
Statele Unite ale Americii
IllinoisRemoteNormă întreagăSeniorLimbă Obligatorie: englezăCercetare clinicăOversee 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.
