- 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
- American Medical Association (Chicago, IL)
- Project Specialist II Chicago, IL (Hybrid) The American Medical Association (AMA) is the nation's largest professional Association of physicians and a non-profit ... have an opportunity at our corporate offices in Chicago for a Project Specialist II on our Professional Satisfaction/Practice Sustainability (PS2) team. This is… 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:** ... including the Food and Drug Administration (FDA) and local Institutional Review Board . + Maintains...**Req ID** : 9955 **Working Title** : Research Grant Specialist II (Remote) - Inflammatory Bowel Disease… more
- 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
- ThermoFisher Scientific (Bethesda, MD)
- …Benefits** The hourly pay range estimated for this position Physician Assistant, Specialist II based inMaryland is $128,000.00-$165,000.00. This position may ... trial is conducted under the requirements relating to obtaining informed consent and IRB approval of the protocol. + Reviews and signs-off on regulatory information… more
- Johns Hopkins University (Baltimore, MD)
- …operations of the program. **Specific Duties and Responsibilities** + Assists the Start Up Specialist new study IRB submissions as needed. + Ensures smooth study ... be responsible for study site activation and management, including regulatory review , site study team training, data monitoring and integrity management, patient… more