- Cedars-Sinai (Los Angeles, CA)
- …federal and local agencies including the Food and Drug Administration (FDA) and local Institutional Review Board ( IRB ). **Primary Duties and ... and collaborative, multi-site clinical research. The CCC Clinical Research Specialist II will serve in a cross-functional...including the Food and Drug Administration (FDA) and local Institutional Review Board . + Maintains… more
- 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
- Vanderbilt University Medical Center (Nashville, TN)
- …Research Staff Council monthly meetings. + Attends in-services advertised by the Institutional Review Board , Research Support Services, professional ... and supervision of the Principal Investigator, the Research Nurse Specialist II (RNS II ) is...processes new IRB research proposals, amendments, continuing review applications and adverse events according to institutional… 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:** ... our care the most. **Req ID** : 11255 **Working Title** : Research Grant Specialist II - Department of Medicine - Hybrid **Department** : CSMC 8270111 Medicine -… 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
- 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
- Stony Brook University (Stony Brook, NY)
- …protocol documents when required, manage medical charts, and ensure compliance with all Institutional Review Board policies. The successful incumbent must ... Research Support Specialist **Required qualifications (as evidenced by an attached...research tool. Experience with preparation of regulatory materials (eg, IRB , grant progress reports). Experience with purchasing, and/or budget… more
- Baylor Scott & White Health (Temple, TX)
- …certification optional, but appreciated. + Will assist in development and maintenance of IRB approval in the role of regulatory specialist . + May obtain ... Testing program. + Communicates with IRB and submits IRB documentation as needed (ie, continuing review , KSP) + Any other tasks as assigned by management… 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