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.
Statele Unite ale Americii
CaliforniaLead global clinical operations for Atrium Therapeutics’ RNA therapies targeting cardiomyopathies. Oversee CROs, vendors, budgets, timelines, compliance, and trial delivery.
IsraelRemoteNormă întreagăJuniorNivel mediuLimbă Obligatorie: englezăLimbă Obligatorie: ebraicăCercetare clinicăMonitor 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.
Regatul Unit
Irlanda
Polonia
Africa de SudRemoteNormă întreagăSeniorLimbă Obligatorie: englezăCercetare clinicăLead clinical data standards, quality, and governance for ICON’s sponsor-dedicated trials. Improve global processes and coordinate delivery across teams.
Statele Unite ale Americii
Florida
Kansas
New Jersey
Carolina de Nord
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.
Statele Unite ale Americii
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.
Lead clinical trial analyses, statistical programming, and analysis plan development at Thermo Fisher Scientific. Mentor junior statisticians and coordinate work with sponsors, programmers, and data managers.
Statele Unite ale AmericiiFloridaLa sediuNormă întreagăJuniorLimbă Obligatorie: englezăCercetare clinicăSupport clinical studies across the University of Miami’s academic health system. Coordinate participant screening, study data, regulatory records, and protocol compliance.
Statele Unite ale Americii
KentuckyRemoteNormă întreagăSeniorLimbă Obligatorie: englezăCercetare clinicăMonitor clinical trial sites for CTI, a global clinical research CRO, and oversee site visits, regulatory records, investigational products, and study deliverables. Coordinate site management and study activities with investigators, sponsors, clients, and internal teams.
