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.
Statele Unite ale AmericiiNew YorkSupport cancer research at Memorial Sloan Kettering Cancer Center by collecting clinical data and assisting with patient-facing studies. Maintain accurate research records and coordinate study protocols with research and care teams.
Statele Unite ale AmericiiHibridNormă întreagăJuniorNu este necesară o diplomăLimbă Obligatorie: englezăCercetare clinicăLead infectious disease clinical trials and research projects at Emory University’s Grady Hospital. Coordinate study data, participant recruitment, regulatory compliance, sponsor communications, and staff guidance.
Statele Unite ale AmericiiHibridNormă întreagăJuniorNu este necesară o diplomăLimbă Obligatorie: englezăCercetare clinicăCoordinate infectious disease clinical trials at Emory University School of Medicine, overseeing participant activities, specimens, study records, and regulatory submissions. Support trial operations through database management, protocol compliance, sponsor meetings, and guidance for junior staff.
Statele Unite ale AmericiiHibridNormă întreagăJuniorNu este necesară o diplomăLimbă Obligatorie: englezăCercetare clinicăCoordinate infectious disease clinical trials at Emory University and Grady Hospital, supporting participant recruitment, research data, specimen collection, and study procedures. The role also handles regulatory tracking, quality assurance, and trial documentation.
