- 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
- Boston University (Boston, MA)
- **RESEARCH SPECIALIST II , Department of Global Health** **Job Description** **RESEARCH SPECIALIST II , Department of Global Health** **Category** Boston ... **Salary Grade** Grade 47 **Position Type** Full-Time/Regular he Research Specialist will implement and administer externally funded research studies, primarily… 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
- 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
- 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
- Beth Israel Lahey Health (Boston, MA)
- **Overview** **The Senior Research Administrator, Post-Award (Research Administrator II )** will, under the direction of the Director, Major Projects and Post Award ... and translate financial data so it is understandable for the non- specialist . Investigate any anomalies and provides timely resolutions. Reallocate budgets and… 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
- Colorado State University (Fort Collins, CO)
- Posting Detail Information Working TitleQuality Assurance Specialist III Position LocationFort Collins, CO Work LocationPosition is fully in-office/in-person ... Number202501012AP Position TypeAdmin Professional/ Research Professional Classification TitleProf/Indiv Contrib II Number of Vacancies Work Hours/Week40 Proposed Annual Salary… more
- Veterans Affairs, Veterans Health Administration (Ann Arbor, MI)
- Summary The Clinical Pharmacy Specialist (CPS) functions at the highest level of clinical practice, works independently under their scope of practice to directly ... care for patients. The Clinical Oncology and Hematology Pharmacist Specialist must be a licensed pharmacist, preferably with a Pharm.D., and have completed a… 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
- 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