Monitor Roche-sponsored clinical trials for a contract research organization, supporting site compliance, accurate data, complete documentation, and trial progress.
Združene države Amerike
Minnesota
OhioLead Medtronic’s global clinical evidence strategy for peripheral nerve stimulation therapies throughout the product lifecycle. Oversee premarket and postmarket research supporting scientific, regulatory, reimbursement, and commercial goals.
TajvanHibridnoPolni delovni časJuniorSrednja ravenZahtevani Jezik: angleščinaZahtevani Jezik: kitajščinaKlinične raziskaveSupport Emerald Clinical’s global early-phase trials across APAC. Coordinate study records, meetings, budgets, vendors, and trial master file activities.
Use R and Shiny to explore clinical trial data and build interactive visualizations. Support Syneos Health’s life sciences clients with reproducible analyses and insights for clinical decisions.
Združene države Amerike
KalifornijaLead global clinical operations for Atrium Therapeutics’ RNA therapies targeting cardiomyopathies. Oversee CROs, vendors, budgets, timelines, compliance, and trial delivery.
IzraelNa daljavoPolni delovni časJuniorSrednja ravenZahtevani Jezik: angleščinaZahtevani Jezik: hebrejščinaKlinične raziskaveMonitor clinical trial sites across Israel for Thermo Fisher Scientific’s PPD services, supporting protocol compliance, data quality, documentation, and audit readiness.
Join Syneos Health’s Clinical Solutions team as a Principal Biostatistician, supporting life sciences and clinical development services. Use biostatistical and drug development expertise to help customers advance drug development and commercialization.
Združeno kraljestvo
Irska
Poljska
Južnoafriška republikaNa daljavoPolni delovni časSeniorZahtevani Jezik: angleščinaKlinične raziskaveLead clinical data standards, quality, and governance for ICON’s sponsor-dedicated trials. Improve global processes and coordinate delivery across teams.
Združene države Amerike
Florida
Kansas
New Jersey
Severna Karolina
UtahMonitor clinical trial sites and support protocol compliance, patient recruitment, and study documentation for IQVIA. Coordinate with site staff and project teams to help trials meet quality standards and milestones.
Združene države Amerike
MassachusettsNew Jersey
New YorkSupport Regeneron clinical trial teams by coordinating study data, sites, reporting, and close-out activities. Help keep studies on track from site activation through completion.
