- Mount Sinai Health System (New York, NY)
- …in the preparation and submission of grant applications and documents (eg, Institutional Review Board , Grants and Contracts Office). **Qualifications** ... The Clinical Research Coordinator is an entry human subjects researcher, responsible for conducting and...telephone calls. + Assists in the collection, analysis and review of experimental data for publication and presentation. +… more
- MetroHealth (Cleveland, OH)
- …coordinator working with human subjects . Experience working with an Institutional Review Board ( IRB ). Good organizational and problem-solving ... other related field. Three years of experience working as a clinical research coordinator working with human subjects , or two years of experience and one of… more
- University of Utah (Salt Lake City, UT)
- …and regulatory issues associated with human research protections and compliance for the Institutional Review Board ( IRB ). Provides direct ... Details **Open Date** **Requisition Number** PRN39884B **Job Title** Institutional Review Board Adm...Plans, develops and administers comprehensive educational programs pertaining to human research protections and IRB review… more
- Colorado State University (Fort Collins, CO)
- …with applicable regulations and guidelines Position Summary The Senior Institutional Review Board ( IRB ) Coordinator will serve as a contact and ... facilitate the review of research protocols involving human subjects . This position provides education and...and by CSU IRB policies. The Senior IRB Coordinator facilitates the research review… more
- Georgetown Univerisity (Washington, DC)
- …confirmation letters after review . + Complete GU Local IRB review for local consideration compliance. + Execute institutional clearance letter and ... IRB regulations. The IRB Reliance Coordinator will oversee activities related to institutional ...A minimum of one year work experience must include: human subjects ' review /oversight; interaction with… more
- Dartmouth Health (Lebanon, NH)
- …regulatory agencies. * May maintain study and regulatory documentation including working with the Institutional Review Board ( IRB ), ensuring all staff ... new clinical research coordinator staff onGood Clinical Practice (GCP), Human Subjects Protection (HSP) practices,the ethical conduct of research and… more
- University of Washington (Seattle, WA)
- …System. + Work with Regulatory Coordinator to ensure that reports to the Institutional Review Board , FDA, and/or study sponsors are timely, accurate, and ... within the University system (eg Grant and Contract Services, Institutional Review Board , Office of...of Health (NIH) regulations pertaining to clinical research in human subjects . + Design, develop, document and… more
- University of Washington (Seattle, WA)
- …of submission and continuous reporting to the relevant regulatory agencies, including the Institutional Review Board , the Food and Drug Administration (FDA), ... bodies. These include but are not limited to the Institutional Review Board , the ...FDA, GCP, and NIH requirements relating to research involving human subjects . * Experience using electronic data… more
- University of Washington (Seattle, WA)
- …* Work with the Regulatory Coordinator to ensure that reporting to the Institutional Review Board and study sponsors are timely, accurate and satisfy ... implementing multiple research projects to test the hypotheses in human subjects . **Position Complexities** This position requires...within the University system (eg Grant and Contract Services, Institutional Review Board , Office of… more
- University of Washington (Seattle, WA)
- …qualitative and quantitative research and data collection * Experience developing and submitting Institutional Review Board ( IRB ) proposal and ... Medicine, has an outstanding opportunity for a full-time Research Coordinator .** The Research Coordinator will work under...to ensure data quality * Conduct data collection and human subjects research activities (eg, moderate focus… more
- Stanford University (Stanford, CA)
- …for completion and accuracy with source documents. Prepare regulatory submissions, and ensure institutional Review Board renewals are completed. + Assemble ... Clinical Research Coordinator Associate **School of Medicine, Stanford, California, United...IRB . Protect the rights, safety and well-being of human subjects involved in the clinical trials.… more
- University of Pennsylvania (Philadelphia, PA)
- …data collection and data entry. Responsible for the preparation and processing of all Institutional Review Board ( IRB ) documentation through the ... resources, and much more. Posted Job Title Clinical Research Coordinator B/C (Department of Pulmonary, Allergy and Critical Care)...of a team, as well as independently; knowledge of IRB and human research protection regulations; prior… more
- Texas Tech University Health Sciences Center - El Paso (El Paso, TX)
- …**Major/Essential Functions:** + Complete research applications and submit updated documentation through the institutional Review Board ( IRB ) + Advising ... personnel in preparing research protocols and subsequent submission for IRB review . + Maintaining IRB ...University and research institution contracts. + Research experience with human subjects . + Experience with IRB… more
- University of Utah (Salt Lake City, UT)
- …with the preparation and submission of grant applications and regulatory documents (eg, Institutional Review Board , Grants and Contracts Office). This work ... Date** 05/31/2024 **Requisition Number** PRN14882N **Job Title** PS Study Coordinator **Working Title** PS Study Coordinator **Job... IRB CITI Course in the Protection of Human Research subjects certificate obtained within six… more
- Dartmouth Health (Lebanon, NH)
- …standards operating procedures for the execution of clinical trial operations, including timely Institutional Review Board ( IRB ) submissions meeting ... for the ethical conduct of research, and safeguards for protection of human subjects especially when conducting research with vulnerable populations. *… more
- University of Washington (Seattle, WA)
- …for upcoming study appointments + Assist in preparation of Human Subjects Division/ Institutional Review Board applications and modifications ... (DAID) has an outstanding opportunity for a **full-time Research Coordinator .** This position will support the Chu Lab in...up to date + Knowledge and prior experience with human subjects institutional review… more
- Hackensack Meridian Health (Edison, NJ)
- …documentation such as protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, and progress reports. ... within the protocol. + In collaboration with the principal investigator, clinical research coordinator , and clinical team, participates in the review of studies… more
- University of Massachusetts Amherst (Amherst, MA)
- …and track participant compensation utilizing appropriate University guidelines. + Assist with Institutional Review Board ( IRB ) protocol submission ... to participant recruitment and screening. + Assist with administrative tasks related to human subjects research: eg, assist with the construction of Site… more
- Stanford University (Stanford, CA)
- …for completion and accuracy with source documents. Prepare regulatory submissions and ensure institutional Review Board renewals are completed. + Assemble ... Clinical Research Coordinator Associate **School of Medicine, Stanford, California, United...IRB . Protect the rights, safety and well-being of human subjects involved in the clinical trials.… more
- Baptist Memorial (Memphis, TN)
- …for and the conduct of research. + Implements, coordinates, manages and reports to the Institutional Review Board ( IRB ). + Implements, coordinates and ... IRB , study sponsors, and all investigators. The research coordinator I will collaborate with research coordinators, data managers...the research. + Serves as an advocate for the human subjects by establishing and maintaining compliance… more