- Cedars-Sinai (Los Angeles, CA)
- …and local agencies, including the Food and Drug Administration (FDA) and local Institutional Review Board . Primary Duties and Responsibilities: + ... ready to be a part of breakthrough research?** The Clinical Research Data Specialist II independently manages data for assigned research studies, demonstrating a… more
- Cedars-Sinai (Los Angeles, CA)
- …local agency requirements including the Food and Drug Administration (FDA) and local Institutional Review Board . **Primary Job Duties and Responsibilities:** ... care the most. **Req ID** : 11255 **Working Title** : Research Grant Specialist II - Department of Medicine - Hybrid **Department** : Medicine - Admin **Business… more
- Huron Consulting Group (Van Buren, AR)
- …concurrently and apply your expertise and work ethic to process and review Institutional Review Board ( IRB ) submissions and conflict of interest ... IRB members, subjects, and other individuals) and COI disclosures. + Conducts pre- review of IRB submissions to determine federal agency oversight, evaluate… more
- University of Maryland, Baltimore (Baltimore, MD)
- …research to meet changing needs and requirements and enforces standards. Prepares for the Institutional Review Board ( IRB ) and Health Insurance ... University of Maryland, Baltimore (UMB)*is currently seeking a*Lead Clinical Research Specialist *to join the*School of Medicine - Radiation Oncology.*The mission of… more
- Methodist Health System (Dallas, TX)
- …the IRB . * Create and/or adapt clinical trial informed consent documents for Institutional Review Board ( IRB ) submission. * Maintain regulatory ... Shift :** **Job Description :** Your Job: The Regulatory Specialist will perform expertise in the regulatory component of...research trials to include, but not limited to; Phase II and IV clinical, investigator initiated trials (IITs), and… more
- University of Pennsylvania (Philadelphia, PA)
- …wellness programs and resources, and much more. Posted Job Title Research Specialist B/C/D ( Infectious Diseases Division of Emergency Medicine) Job Profile Title ... Research Specialist B Job Description Summary The Research ...study operations including maintaining study databases, compliance with all IRB and regulatory documentation, and assisting with the preparation… 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
- Hartford HealthCare (Hartford, CT)
- …portfolio of cancer research studies. In compliance with all regulatory, institutional and departmental requirements, performs patient screening, data collection and ... monitoring of protocol for compliance and patient safety; source document review ; data entry; sponsor monitoring. * Interact/collaborate with all physicians, other… more
- Stony Brook University (Stony Brook, NY)
- …of patient eligibility for protocol participation by way of chart review , data collection and patient evaluation/assessment identification. In addition, the ... reporting all adverse drug reactions to the FDA, NCI, Oncology cooperative groups, IRB and sponsoring drug companies. Lastly, they will conduct patient and staff… more
- Stanford Health Care (Palo Alto, CA)
- …the supervising physician, enrolls patients in investigational studies approved by the Investigational Review Board ( IRB ), and orders the necessary tests and ... with the attending physician. Other responsibilities include consultation with specialist providers and other team members regarding findings/changes in patient… more