Lead multidisciplinary medical device studies for NAMSA, a global MedTech development services company. Oversee sites, regulatory deliverables, data quality, clinical reporting, and study execution.
Contract 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.
Contract 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.
Monitor 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.
United States
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.
Coordinate 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.
Lead 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.
Monitor sponsor-dedicated clinical trials for ICON, a global clinical research organization. Support protocol compliance, reliable data, and patient safety across Canadian trial sites.
Lead regional oncology clinical trial delivery for BeOne Medicines, coordinating operations, vendors, timelines, budgets, quality, and regulatory execution across assigned countries.
United States
MassachusettsNew Jersey
North Carolina
Ohio
Pennsylvania
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.
Lead 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.
Lead 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.
Lead scientific contributions to CSL’s hematology clinical development programs. Support study execution, clinical data interpretation, regulatory documentation, medical monitoring, and external oversight committees.
Monitor 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.
Parexel 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.
Support Parexel pharmaceutical clinical trials through data review, medical monitoring, and study operations. Help protocol leads and stakeholders deliver compliant clinical studies.
