- University of Rochester (Rochester, NY)
- …University of Rochester is seeking a part-time (20 hours/week) Human Subject Research Specialist , Level II , to coordinate human subject research activities. The ... participant adherence with protocol requirements. - Participates in the development, review and approval of case report forms (CRFs) and study-specific procedure… more
- University of Rochester (Rochester, NY)
- …managing and supervising staff, working with familycaregiversand/orproviders, preparing and managing Institutional Review Board documentation preferred. + ... and performance. Manages regulatory paperwork in accordance with human subject IRB , continuing education, clinical trial, and grant agency requirements and… more
- Stony Brook University (Stony Brook, NY)
- …Investigational New Drug (IND) and Investigational Device Exemption (IDE) applications. + Creating Institutional Review Board ( IRB ) submissions and ... Investigator Initiated Trial Specialist - Clinical Trials **Position Summary** The Cancer...managing correspondence across research sites, particularly in single- IRB /multi-site studies. + Planning and implementing changes to the… more
- University of Rochester (Rochester, NY)
- …the research team. May provide mentorship to Human Subject Research Specialist I. **ESSENTIAL FUNCTIONS** **Study Visits:** Recruits, consents, schedules, and ... and communicating as needed. **Mentoring:** Mentors and trains Human Subject Research Specialist I (HSRS I) on activities related to conducting human subject… more
- University of Rochester (Rochester, NY)
- …documentation, including study protocols, consent forms, logs, certifications, labs, IRB and sponsor documents, and applicable communication. Manages and submits ... amendments and continuing reviews for IRB approval. + Ensures compliance with all applicable regulatory...approval. + Ensures compliance with all applicable regulatory and institutional requirements and standards. Trains with and assists other… more
- Stony Brook University (Stony Brook, NY)
- …Qualifications:** Oncology and/or chemotherapy experience. Clinical trials research experience. IRB research training. **Brief Description of Duties:** The Cancer ... at ### or visit OEA (https://www.stonybrook.edu/commcms/oea/) . _In accordance with the Title II Crime Awareness and Security Act_ a _copy of our crime statistics… more
- Stony Brook University (Stony Brook, NY)
- …drafts and/or manuscripts based on the collected data. + Assist with the preparation of Institutional Board Review ( IRB ) applications and documents. + ... research studies and clinical trials per federal, state, and institutional guidelines. Under supervision, the Specialist collects,...or for a maximum of 90 days. An initial review of all applicants will occur two weeks from… more