- Stony Brook University (Stony Brook, NY)
- …clinical/pre-clinical studies, setting up study protocols with Institutional Review Board ( IRB ), Radioactive Drug Research Committee (RDRC) and FDA ... development of junior members. SBU is committed to neuroimaging research . Our infrastructure now includes: an onsite cyclotron, a...for internal and external presentation. * Correspond with the IRB and RDRC for existing and new PET studies.… more
- Mount Sinai Health System (New York, NY)
- …assistance and guidance in the preparation of budgets, Grants and Contracts Office/ Institutional Review Board paperwork, application forms, no-cost ... Ensures that the administration of sponsored programs related to research is in compliance with federal , state...(ie, IRB ; Financial Conflict of Interest in Research Committee) for review . + Acts as… more
- Mount Sinai Health System (New York, NY)
- …study information. Assists in preparing grant applications and documents (for eg, Institutional Review Board , Grants and Contracts Office). ... **Job Description** The Clinical Research Coordinator assists in the daily activities of...is an equal opportunity employer, complying with all applicable federal civil rights laws. We do not discriminate, exclude,… more
- SUNY Upstate Medical University (Syracuse, NY)
- … guidelines. Interact and correspond with clinicians, sponsors, cooperative groups, Upstate's Institutional Review Board and regulatory agencies. Enroll, ... Job Summary: Coordinate various research trials for the Institute for Global Health,...register and screen patients for clinical research trials; collect and submit clinical trial patient data.… more
- University of Rochester (Rochester, NY)
- …Provides study-specific training, oversight, and back-up support. + Trains on federal , state, sponsor, and/or institutional regulations, policies, and practices ... is identified **Liaison:** Serves as the liaison between cross-functional research team, study sponsors, and IRB to...order to keep current with Good Clinical Practice guidelines, federal and state polices and laws, institutional … more
- Rochester Institute of Technology (Rochester, NY)
- …with coordinating inter- institutional agreements and related issues including single IRB and human subjects review on multi-institution projects, as well ... university support offices to enhance, update, and coordinate university research compliance resources and practices required by federal...and implementation of the Office of the VP for Research and institutional research non-financial… more
- Stony Brook University (Stony Brook, NY)
- …Oncology/Chemotherapy experience. Research experience coordinating clinical trials and IRB research training. **Special Notes** **:** **Resume/CV should be ... Research Nurse - Cancer Clinical Trials **Position Summary**...patient eligibility for protocol participation by way of chart review , data collection and patient evaluation/assessment identification. In addition,… more
- University of Rochester (Rochester, NY)
- …and internal equity considerations._ **Responsibilities:** GENERAL PURPOSE The Human Subject Research Specialist I (HSRS I) plays a vital role in contributing ... and audit preparation in addition to supporting the broader research team through staff training and oversight. The HSRS...clarification as needed. + Verify study related information and review subject records to ensure complete and accurate data.… more
- Weill Cornell Medical College (New York, NY)
- …submits for review /approval and maintains correspondence with sponsoring agency, IRB and collaborative institutions. + Maintains research effort tracking for ... Title: Assistant Research Coordinator Location: Upper East Side Org Unit:...marital status, or any other characteristic protected by applicable federal , state, or local law. Cornell University embraces diversity… more
- Kelly Services (Rye Brook, NY)
- …clinical database. + Support and adhere to Good Clinical Practices (GCP) guidelines, FDA, Institutional Review Board ( IRB ) and HIPAA regulations, Site ... and medical outcomes for oncology patients. Responsible for the collection and review of clinical protocol research data; Interpretation of data (including… more