Statele Unite ale Americii
OhioHibridNormă întreagăNivel mediuSeniorLimbă Obligatorie: englezăCercetare clinicăSupport clinical trial data coordination and case report form management across research studies at University Hospitals Case Medical Center. Help maintain accurate, compliant, and secure clinical research records.
Statele Unite ale AmericiiLead multidisciplinary medical device studies for NAMSA, a global MedTech development services company. Oversee sites, regulatory deliverables, data quality, clinical reporting, and study execution.
Statele Unite ale Americii
MarylandContract Senior Clinical Research Associate overseeing clinical trial sites for Lotus Clinical Research. The role covers GCP compliance, essential documentation, investigational product accountability, and study close-out.
Statele Unite ale AmericiiMarylandContract Senior Clinical Research Associate responsible for monitoring clinical-trial sites and supporting study execution. Ensures compliance with GCP, FDA, ICH, protocol, and study-document requirements through site visits.
FranțaHibridNormă parțialăSeniorLimbă Obligatorie: englezăLimbă Obligatorie: ebraicăCercetare clinicăMonitor investigational sites across clinical trial phases while maintaining GCP compliance and data quality. Support Allucent’s biopharmaceutical clients with site activation, regulatory activities, and study startup.
Statele Unite ale Americii
New JerseyLead and oversee late-phase endocrine clinical trials at Ascendis Pharma in a hybrid Princeton role. Analyze clinical data, support regulatory submissions, and advance therapies addressing unmet medical needs.
Statele Unite ale AmericiiLa sediuNormă întreagăNivel mediuSeniorLimbă Obligatorie: englezăCercetare clinicăCoordinate oncology clinical trials at UAMS, supporting participant care, protocol compliance, research data, and collaboration among investigators, sponsors, and clinical teams.
Senior Clinical Research Associate II overseeing UK clinical trial sites for CTI Clinical Trial and Consulting Services. The role includes site visits, remote monitoring, enrollment support, and regulatory compliance.
CanadaStatele Unite ale Americii
PennsylvaniaRemoteNormă întreagăSeniorLimbă Obligatorie: englezăCercetare clinicăLead clinical trial delivery for ICON, overseeing study start-up, execution, compliance, risk management, budgets, and closeout. Partner with sponsors and study teams to deliver high-quality research programs.
CanadaMonitor sponsor-dedicated clinical trials for ICON, a global clinical research organization. Support protocol compliance, reliable data, and patient safety across Canadian trial sites.
Statele Unite ale AmericiiLead regional oncology clinical trial delivery for BeOne Medicines, coordinating operations, vendors, timelines, budgets, quality, and regulatory execution across assigned countries.
Statele Unite ale Americii
MassachusettsNew Jersey
Carolina de NordOhioPennsylvania
TennesseeLead country-level operations for complex oncology clinical trials at IQVIA in Durham, coordinating sites, vendors, recruitment, compliance, budgets, and patient safety. The role serves as the primary sponsor contact and operational lead for high-priority or high-risk studies.
Monitor oncology and specialty clinical trials remotely for Parexel as a Clinical Research Associate. Oversee sites, compliance, recruitment, data quality, and participant safety.
Lead oncology clinical trials for Parexel from a home-based UK role. Manage vendors, sites, CRAs, regulatory compliance, study documentation, and trial delivery.
Statele Unite ale AmericiiLead clinical data acquisition for Devoted Health’s older-member care by improving healthcare data exchange and usability. Manage integrations, data-gap analysis, vendor partnerships, interoperability initiatives, and performance measurement.
Statele Unite ale AmericiiLead regional oncology clinical trial delivery for BeOne Medicines across timelines, sites, vendors, budgets, compliance, and operational teams. Oversee study execution from feasibility through closeout while maintaining quality and inspection readiness.
Statele Unite ale AmericiiMassachusettsPennsylvaniaLa sediuNormă întreagăLiderLimbă Obligatorie: englezăCercetare clinicăLead scientific contributions to CSL’s hematology clinical development programs. Support study execution, clinical data interpretation, regulatory documentation, medical monitoring, and external oversight committees.
Statele Unite ale Americii
TexasRemoteNormă întreagăJuniorNivel mediuLimbă Obligatorie: englezăCercetare clinicăMonitor sponsor-dedicated clinical trial sites for ICON Strategic Solutions while supporting regulatory compliance, patient safety, data quality, and site performance. This role serves as a key link between study sponsors and investigational sites.
Lead end-to-end clinical trial delivery for ICON plc, including study oversight, enrollment, budgets, start-up, and regulatory compliance. Guide cross-functional teams and support successful outcomes across complex clinical research programs.
CanadaRemoteNormă întreagăSeniorLimbă Obligatorie: englezăLimbă Obligatorie: francezăCercetare clinicăParexel is hiring a senior bilingual Clinical Research Associate to monitor clinical trials across Canada. The role manages site relationships, compliance, data quality, and study execution from site identification through close-out.
