- 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
- 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
- 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
- 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
- Johns Hopkins University (Baltimore, MD)
- …operations of the program. **Specific Duties & Responsibilities** + Assists the Start Up Specialist new study IRB submissions as needed. + Ensures smooth study ... Research Program Manager, we are seeking a **_Sr. Research Program Coordinator II who_** will be responsible for study site activation and management, including… 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
- Children's Hospital Boston (Boston, MA)
- …Posting Title:Clinical Research Specialist IDepartment:Pediatrics-Hematology/Oncology AutoReqId:80802BRStatus:Full-TimeStandard Hours per Week:40 Job Posting ... of the PI, coordinates preparation of protocol applications for submission to the IRB , sponsor, or regulatory authority. As directed by the PI corresponds with the… 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