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Showing 41-60 of 954
Irb Manager jobs

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NYU School of MedicineNew York, NY

Oversee and ensure staff IRB, NYUSOM Finance, Sponsored Programs and Office of Clinical Trials, and Office of Industrial Liaison regarding new protocol...

Aventura Hematology & Oncology Services, United States-New Jersey-Edison-HCAPS-ICC at NJ - JFK Medical Center, United States-Florida-West Palm Beach-JFK Medical Center North CampusAventura, FL

Ensure site IRB approval is current and all IRB documentation is in order. To be accompanied by Project Manager, Project Lead, or CRA Manager on selected visits...

System OneSummit, NJ

BA / BS Minimum 6 years clinical study management experience (involved in the protocol implementation team) at a CRO or Pharma/Biotech with at least 2 years

City Of HopeDuarte, CA

The Business Manager supports multiple faculty members, postdoctoral fellows and research associates within the Hematologic Malignancies and Stem Cell...

The McConnell Group, IncFairfield, MD

Collect, sort, and file all signed consent forms and completed questionnaires in compliance with procedures established by the Internal Review Board (IRB) and...

NYU School of MedicineNew York, NY

IRB/OCT Develops new IRB protocols with research staff and oversees Research Coordinators efforts regarding IRB submission and renewals....

Duke UniversityDurham, NC

Time off requests will be submitted to your manager per departmental & Duke Policy. Communicate frequently with your manager, keeping them up-to-date on your...

Northwell HealthManhasset, NY

Become proficient in use of IRB Manager, RedCapand other HIPAA compliant databases for data input and management....

NYU School of MedicineNew York, NY

Along with Informatics Manager, providing technical assistance to CTSI Program Directors and staff in accessing and interfacing with institutional data sources...

NYU School of MedicineNew York, NY

The candidate will serve as a liaison between the sponsor, CRO, IRB and internal departments/ staff. Reporting to the Senior Manager of Regulatory Affairs Unit,...

miRagen TherapeuitcsBoulder, CO

Assists in the preparation, handling and tracking of site IRB submissions. Supports Clinical Trial Managers in updating study plans and ensuring integrity...

Advanced ClinicalEast Hanover, NJ

Ensure study ICF-template for central IRB sites contain the approved pre-negotiated language. Interface with the clinical sites, IRBs, the portfolio Specialists...

The Outsource Group - Kaiser Permanente Oakland, United States-New Jersey-Edison-HCAPS-ICC at NJ - JFK Medical Center, United States-Florida-West Palm Beach-JFK Medical Center North CampusOakland, CA

Ensure site IRB approval is current and all IRB documentation is in order. To be accompanied by Project Manager, Project Lead, or CRA Manager on selected visits...

City Of HopeDuarte, CA

Endnote or other reference manager. May include their associated materials (letters of intent, consent documents, patient materials, IRB application, etc.)....

VanderHouwenBothell, WA

Manager Regulatory AffairsOur client is a global medical device company focused on supporting customers by being their trusted partner, delivering high-quality...

City Of HopeDuarte, CA

Retain and develop Managers and RPAs for the IRB and CPRMC/PRMC. Certified IRB Professional is preferred. Retain and develop quality committee managers who...

Kelly ServicesEast Hanover, NJ

Ensure study ICF-template for central IRB sites contain the approved pre-negotiated language. Interface with the clinical sites, IRBs, the portfolio Specialists...

Miami Children's HospitalMiami, FL

Manages and actively participates in the day-to-day Regulatory Affairs activities including communications with the IRB, investigators, Sponsors, and internal...

NYU School of MedicineNew York, NY

Respond to IRB queries from enrolling center after consultation with CRA and/or PM. This position will report directly to the Project Manager and the Program...

City Of HopeDuarte, CA

Oversee and maintain documentation of correspondence to and from the IRB. Assist COH researchers in study design, consent form creation and compliance with IRB...


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