- Mount Sinai Health System (New York, NY)
- …required in project coordination, especially related to research projects and IRB preferred. **Responsibilities** + Establishes the coordination of complex project ... Vice Chair of the Department of Public Health. + Will coordinate and monitor IRB and related activities for research focused projects. + Develops and maintains a… more
- University of Rochester (Rochester, NY)
- …of data and obtains clarification as needed. + Verify study related information and review subject records to ensure complete and accurate data. + Enter data into ... database. Run reports from database and prepare documents for IRB , NIH and DSMB reporting. + Oversee data cleaning...members data collection forms). + Oversee audit preparations for IRB /NIH (ensuring information and subject files are up to… more
- University of Rochester (Rochester, NY)
- …of expertise. This requires consulting with investigators, research personnel, review specialists, Board Members, and University offices/departments, Sponsors, ... activities at sites and with public speaking required. + Experience working in an IRB and managing an educational program is preferred. + Excellent oral and written… more
- New York University (New York, NY)
- …input them on Qualtrics for electronic versions. * Assist PI in submitting IRB applications and modifications, as needed. * Assist in participant recruitment and ... experience in motivational interviewing theory and techniques. * Knowledge of IRB protocols and procedures to modify protocols. Performance Evaluation Procedure *… more
- University of Rochester (Rochester, NY)
- …oversight, and back-up support. + Trains on federal, state, sponsor, and/or institutional regulations, policies, and practices related to human subject research. + ... + Manages and submits study applications, amendments, and continuing reviews for IRB approval + Ensures compliance with all applicable regulatory and … more
- Touro University (Hawthorne, NY)
- …pre-clinical trial set up, initial and ongoing regulatory submission and IRB activities, subject screening and enrollment, specimen collection and transmittal, data ... team and clinical research nurses and team. Responsibilities + Assist in new IRB application and annual renewal process of COG, sponsored, local and other multi-… more
- Weill Cornell Medical College (New York, NY)
- …response. + Assess patient eligibility for inclusion in investigational studies. Review patient history and abstracts and records information; records pre-study lab ... baseline laboratory blood work from patient and arrange necessary scans. + Review "informed consent" with patient; coordinate and educate patient and medical… 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 ... Responsibilities:** + Oversee the Conflict of Interest process for researchers including review of all project COIs, drafting of management plans or addressing… more
- Research Foundation CUNY (New York, NY)
- …facilitates meetings between the CEC Core Directors and the Community Advisory Board (CAB). Engages the CAB to plan academic-community education sessions, and ... all regulatory requirements pertaining to research projects involving human subjects, including IRB approvals & Amendments and the secure storage of subject data.… more
- SUNY Upstate Medical University (Syracuse, NY)
- …all managed studies. The CRA I will interact daily with clinicians, sponsors, IRB , regulatory agencies and other research professionals. This is a subject / patient ... will be responsible for all aspects of the trial conduct including; IRB submission, regulatory documents, training staff, overseeing enrollment of appropriate study… more