- University of Rochester (Rochester, NY)
- …Vision & Psychosis Lab at the University of Rochester is searching for a full-time Human Subjects Research Coordinator who will contribute to a federally ... updating study databases (ie, REDCap); (d) preparing materials for IRB review ; (e) delegating responsibilities to other...and co-workers in a sensitive and caring manner. The Research Assistant must complete the Human Subjects… more
- University of Rochester (Rochester, NY)
- …+ Under the direction of the Principal Investigator, assists in the conduct of research studies beginning with the preparation of IRB materials through the ... GENERAL PURPOSE: Plans, coordinates and conducts/implements all research activities associated with the development of patient and caregiver reported outcome… more
- National Institutes of Health (Montgomery County, MD)
- Summary This Program Specialist position serves as an Institutional Review Board ( IRB ) Coordinator , with responsibility for assisting with ... protocols for completeness, accuracy, and compliance with federal regulations and institutional policies; monitoring human subject research protocols; and… more
- HCA Healthcare (Plano, TX)
- …where diversity and inclusion thrive? Submit your application for our Institutional Review Board ( IRB ) Coordinator opening with Medical City ... coordinates complex and broad administrative matters for the Institutional Review Board ( IRB...Assists in the identification of potential regulatory issues with human research protocols, provides technical support and… more
- The Mount Sinai Health System (New York, NY)
- …Assists in the preparation and submission of grant applications and documents (eg, Institutional Review Board , Grants and Contracts Office). **Strength ... The Clinical Research Coordinator is an entry human subjects researcher, responsible for conducting and assisting in clinical research studies under the… more
- The Mount Sinai Health System (New York, NY)
- …Assists in the preparation and submission of grant applications and documents (eg, Institutional Review Board , Grants and Contracts Office). **Strength ... The Clinical Research Coordinator is an entry human subjects researcher, responsible for conducting and assisting in clinical research studies under the… more
- University of Rochester (Rochester, NY)
- …current CITI credentials for Human Subject Protection, GCP, Clinical Research Coordinator , plus additional sponsor GCP certifications as required. (5%) ... POSITION SUMMARY: Coordinates the activities associated with human subject research . Provides assistance to...and publications. (20%) Serves as the liaison between cross-functional research team, study sponsors, and IRB to… more
- Georgetown Univerisity (Washington, DC)
- …Protection - Georgetown University Job Overview The Institutional Review Board ( IRB ) Reliance Coordinator is responsible for the management and ... IRB Reliance Coordinator - Office of Human Subjects...review + Complete GU Local IRB review for local consideration compliance + Execute institutional… more
- UTMB Health (Galveston, TX)
- …or equivalent, and two years of directly related experience. **Job Description:** The Clinical Research Coordinator obtains human subject data for clinical ... IRB , OCR or OSP under direction of research coordinator under the direction of the...eg, submitting a protocol amendment, protocol deviation, and continuing review . + Under direction of PI may draft various… more
- University of Rochester (Rochester, NY)
- …or an equivalent combination of education and relevant experience required. + Experience as Human Subject Research Coordinator I preferred + Knowledge of ... word processing and data analysis software required + Professional Research Coordinator Certification (ie, SoCRA or ACRP) preferred The University of Rochester… more
- MD Anderson Cancer Center (Houston, TX)
- …guidance and support to the Institutional Review Board (s) ( IRB ). The IRB Coordinator is responsible for processing submissions according to ... The IRB Coordinator provides regulatory expertise,...Bachelor's degree. **Experience** **Required:** One year of experience in IRB administration, clinical research or human… more
- Dartmouth Health (Lebanon, NH)
- …Provides regulatory expertise, guidance and administrative support to the Dartmouth-Hitchcock (D-H) Institutional Review Board (s) ( IRB ). Responsible for ... to the policies and procedures outlined in the D-H Human Research Protection Program (HRPP) Toolkit and...Escalates matters of concern to the HRPP Director or IRB Manager as appropriate. * Conducts non-committee review… more
- University of Rochester (Rochester, NY)
- …activities, reporting adverse events to senior study staff, Research Manager, PI, Institutional Review Board ( IRB ), Sponsor, and/or any other ... data entry, and performing medical chart reviews. They will review study protocols, ensure thorough understanding and communication, respond...degree required + Completion of 6 months in the Human Subject Research Coordinator Trainee… more
- Children's Hospital Boston (Boston, MA)
- …participates in the planning, organization, and conduct of audits to evaluate whether the Institutional Review Board ( IRB ) and investigators adequately ... relevant regulations and institutional policies governing the review of human subject research ....requested by the IRB , Department Chair/Chief or Institutional Official to address a Human … more
- Leidos (Dayton, OH)
- …Look no further than Leidos! We are seeking a Research Coordinator - Institutional Review Board ( IRB ) Administrator to support intramural ... Provide IRB management and coordination for intramural human use research working with PIs and...field. + 4 or more years of experience in IRB review ; including IRB communications… more
- University of Pennsylvania (Philadelphia, PA)
- …as part of a team, as well as independently; knowledge of IRB and human research protection regulations Coordinator A: Bachelor's degree required and 1-2 ... and resources, and much more. Posted Job Title Clinical Research Coordinator A/B Job Profile Title Clinical...FDA and other entities + Correspond regularly with the Institutional Review Board and other… more
- University of Rochester (Rochester, NY)
- …interventional activities, to document adverse events and report to senior study staff, PI, Institutional Review Board ( IRB ), Sponsor, and/or any other ... forms and CRFs, are complete, accurate, and available for review . Communicates with Sponsor to clarify data queries to...Associate's degree and completion of 6 months in the Human Subject Research Coordinator Trainee… more
- University of Rochester (Rochester, NY)
- …interventional activities, to document adverse events and report to senior study staff, PI, Institutional Review Board ( IRB ), Sponsor, and/or any other ... forms and CRFs, are complete, accurate, and available for review . Communicates with Sponsor to clarify data queries to...degree and completion of 6 months in the CTSI Human Subject Research Coordinator Trainee… more
- University of Rochester (Rochester, NY)
- …participate in i) budget development, negotiation and implementation, ii) discussions with the human subjects review board and the University's legal office, ... and consent form development, budget development, negotiation and implementation, discussions with the human subjects review board and the University's legal… more
- University of Rochester (Rochester, NY)
- …Communicates adverse events to the PI, documents them as advised and reports them to Institutional Review Board ( IRB ), Sponsor, and/or any other required ... pre-study inspection, initiation, on-going and close out visits). Follow Research Subject Review Board regulations...Associate's degree and completion of 6 months in the Human Subject Research Coordinator Trainee… more