- University of Rochester (Rochester, NY)
- …team in strategy development to ensure workshop success. + Tracks and records regulatory and other documents for the study Evaluating Lethal Means Education Efforts ... + Becomes proficient in the development and/or update of IRB protocols to evaluate new initiatives + Assists in...and Compliance + Tracks study protocol adherence and learn IRB and Sponsor reporting requirements + Assists with data… more
- University of Rochester (Rochester, NY)
- …of expertise. This requires consulting with investigators, research personnel, review specialists, Board Members, and University offices/departments, Sponsors, ... documentation, ensuring compliance with relevant local, state, and federal regulatory requirements. This includes collaboration with OHSP leadership and related… 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
- Mount Sinai Health System (New York, NY)
- …Investigator/Sub-Investigator, Clinical Nurse Manager/Assistant Nurse Manager/Nursing Shift Manager, Investigational Review Board or Patient Relations as needed. ... ensure and procedures. + Engages in formal and informal peer and institutional review processes. + Collaborates with interdisciplinary teams to create… more
- Mount Sinai Health System (New York, NY)
- …to Good Clinical Practice (GCP) guidelines, institutional policies, and applicable regulatory requirements (eg, FDA, IRB , ICH). + Oversee the preparation and ... goals. The Project Manager II will work closely with investigators, research teams, regulatory bodies, and institutional leadership to ensure the success of each… more
- Mount Sinai Health System (New York, NY)
- …study filings. * Maintain source documentation and participant records according to institutional and regulatory requirements. * Stay current on relevant ... II will be responsible for overseeing research operations, ensuring regulatory compliance, maintaining high-quality data standards, and leading staff development… more
- Bausch + Lomb (Albany, NY)
- …the timely coordination and execution of clinical study reports. + Assist in the review of regulatory reports to ensure that reports accurately reflect proper ... evaluation, and selection of CROs and vendors (eg, central labs, central IRB , IVRS, etc.). + Manage the identification, evaluation, and selection of… more
- WMCHealth (Valhalla, NY)
- …applications, amendments, continuing reviews, and informed consent documents for SRC and IRB review and approval. + Establish and maintain regular communication ... of the research department. Responsibilities: + Collect and document patient and regulatory data with exceptional attention to detail, submitting data promptly to… more
- SUNY Upstate Medical University (Syracuse, NY)
- …this role the scope of duties is but not limited to: performance of regulatory tasks including IRB and sponsor/CRO regulatory correspondence, communication ... with IRBs, sponsors, and protocol-related Upstate Departments. Pre-screen, Screen, and enroll research participants in outpatient and inpatient clinical trials, process and ship lab samples, schedule and conduct follow up research appointments for clinical… more
- Stony Brook University (Stony Brook, NY)
- …responsible for developing human clinical research protocols and preparing applications for IRB , RDRC, or IND, collecting PET and/or MRI data, image data analysis, ... analysis * Human clinical research protocol development and preparation for regulatory reviews * Scientific writing, including peer-reviewed publications and grant… more