Jungtinės ValstijosNuotolinisVisas etatasJaunesnysis specialistasVidutinis lygisPrivaloma Kalba: anglųKlinikiniai tyrimaiLead 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.
Jungtinės Valstijos
PensilvanijaCoordinate 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.
KinijaNuotolinisVisas etatasJaunesnysis specialistasVidutinis lygisDiplomas nebūtinasPrivaloma Kalba: anglųKlinikiniai tyrimaiSupport AbbVie oncology trials in China by monitoring clinical sites, managing study risks and helping protect compliance, recruitment and data quality.
BrazilijaNuotolinisVisas etatasJaunesnysis specialistasVidutinis lygisPrivaloma Kalba: anglųKlinikiniai tyrimaiMonitor 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.
Jungtinės ValstijosPensilvanijaCoordinate participant visits, informed consent, data collection, and IRB compliance for University of Pennsylvania clinical studies. Support research activities at study sites in Philadelphia.
Jungtinės ValstijosLead 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.
Jungtinės Valstijos
Kalifornija
Koloradas
MinesotaOversee clinical sites, study documentation, and data quality for Medtronic neurovascular device studies. Coordinate compliant study delivery with investigators, vendors, monitors, and internal teams.
Jungtinės Valstijos
Merilandas
VirdžinijaNuotolinisVisas etatasJaunesnysis specialistasVidutinis lygisDiplomas nebūtinasPrivaloma Kalba: anglųKlinikiniai tyrimaiMonitor 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.
Jungtinės Valstijos
ArizonaNuotolinisVisas etatasJaunesnysis specialistasVidutinis lygisPrivaloma Kalba: anglųKlinikiniai tyrimaiOversee 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.
Jungtinės ValstijosKalifornijaKoloradasMinesotaOversee clinical study sites, data quality, and regulatory records for Medtronic’s neurovascular technologies. Support compliant studies from site activation through closeout.
Jungtinės ValstijosKalifornijaSupport AbbVie’s neurology clinical trials by monitoring research sites and helping uphold regulatory compliance, data quality, patient safety, and recruitment goals.
Jungtinės ValstijosPensilvanijaCoordinate participant screening, study visits, data collection, and regulatory tasks for clinical research at the University of Pennsylvania Perelman School of Medicine.
Jungtinės ValstijosPensilvanijaCoordinate participant visits, study protocols, IRB submissions, and clinical data for the University of Pennsylvania’s medical research programs.
Jungtinės Valstijos
ViskonsinasAnalyze 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.
Jungtinės Valstijos
Naujasis DžersisLead 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.
Jungtinės Valstijos
IlinojusNuotolinisVisas etatasVyresnysis specialistasPrivaloma Kalba: anglųKlinikiniai tyrimaiOversee 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.
