- Vitalief (Livingston, NJ)
- …will support a leading hospital research center in Livingston, NJ, administering and overseeing Institutional Review Board ( IRB ) activities to ensure ... grow sustainably. The Role We are seeking an experienced IRB Coordinator Consultant to join the Vitalief...human subjects research. This role supports investigators, staff, and IRB members in the preparation, review , and… more
- Actalent (Newark, NJ)
- …medication diaries, eligibility checklists, and flow sheets. + Verify Scientific Review Board , Institutional Review Board , data collection plans, and ... staff on available protocols and general research topics such as FDA, IRB , and GCP regulations. Responsibilities + Collaborate with the Protocol Activation office… more
- Vitalief (New Brunswick, NJ)
- …Practice (GCP) guidelines. + Experience in preparation of documents for submission to the Institutional Review Board ( IRB ), continuing reviews, and ... of experience in Clinical Research as a Clinical Research Coordinator , with experience in patient recruiting/pre-screening/consenting/retention; activation; regulatory compliance… more
- Vitalief (Newark, NJ)
- …and achieve sustainable growth. We are seeking a highly motivated Clinical Coordinator to support one of our client's long-term NIH-funded research study focused ... and cognitive factors underlying substance use and abuse. The coordinator will play a central role in managing study...retention throughout the study duration. + Maintain and update IRB protocols, with training and support provided. + Organize… more
- Vitalief (New Brunswick, NJ)
- …patients. We are seeking a talented and enthusiastic Senior Clinical Research Coordinator to join our exceptional team (as full-time, fully benefited Vitalief ... study budget, startup meeting preparation, training staff, and preparation of IRB applications and preparation of regulatory documents, study documents and forms.… more