- 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
- 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** ... **Job Description** The Clinical Research Coordinator is an entry human subjects...telephone calls. + Assists in the collection, analysis and review of experimental data for publication and presentation. +… more
- Boston University (Boston, MA)
- The Human Research Education & QA Coordinator will contribute to the regulatory/ethics/ IRB submission consultations process, ongoing educational ... Research Professionals Network (RPN) Workshops, and Summer Sessions. The Human Research Education & QA Coordinator will perform responsibilities related… more
- University of Utah (Salt Lake City, UT)
- …review and approval of human research protections and compliance for the Institutional Review Board ( IRB ). Responsible for the comprehensive ... institutional processes. **Responsibilities** **Responsibilities:** + Conducts initial review of human research protocol... research protections and IRB review processes for IRB employees, board… 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 ... GENERAL PURPOSE: Assists with the activities associated with human subject research . **RESPONSIBILITIES:** + Assists...and ensures these are complete, accurate and available for review . + Learns and applies the details of the… 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
- University of Colorado (Aurora, CO)
- …**Department: Office of the Vice Chancellor for Research , Colorado Multiple Institutional Review Board , Office of Regulatory Compliance** **Job Title: ... Review Board (COMIRB) is the Institutional Review Board ( IRB...VA Eastern Colorado Health Care System. COMIRB exists to review all proposed human research … more
- University of Colorado (Aurora, CO)
- …**University of Colorado Anschutz Medical Campus** **Department: Colorado Multiple Institutional Review Board (COMIRB)** **Job Title: IRB Review ... and not- human subjects review of research as a designated IRB member. Process... Review Board (COMIRB) exists to review all proposed human research … more
- Mount Sinai Health System (New York, NY)
- …with the preparation and submission of grant applications and regulatory documents (eg, Institutional Review Board , Grants and Contracts Office). This work ... **Job Description** The Clinical Research Coordinator will be involved in...research experience and education + 0-2 years of research / human subjects experience Non-Bargaining Unit, 857 -… more
- University of Rochester (Rochester, NY)
- …works as an integral part of the research team. This role mentors Human Subject Research Coordinator I(s) and supervises students as assigned. **TYPICAL ... institutional regulations, policies, and practices related to human subject research . + Serves as the...combination of education and experience required + Experience as Human Subject Research Coordinator I… 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)
- …with protocol requirements to document adverse events and report to senior study staff, PI, Institutional Review Board ( IRB ), Sponsor, and/or any other ... + Keeps current with all federal, state, sponsor, and institutional policies and laws, standard operating procedures, and guidelines...Associate's degree and completion of 6 months in the Human Subject Research Coordinator Trainee… more
- University of Rochester (Rochester, NY)
- …or an equivalent combination of education and experience required. + Experience as Human Subject Research Coordinator I preferred + Certified Clinical ... GENERAL PURPOSE: The part-time research coordinator (20hrs/wk flexible schedule to...posters, manuscripts, perspective pieces). Additional responsibilities will include writing research protocols, submitting them to the IRB ,… more
- University of Pennsylvania (Philadelphia, PA)
- …as part of a team, as well as independently; knowledge of IRB and human research protection regulations. Coordinator C: A Bachelor's Degree, training as ... and resources, and much more. Posted Job Title Clinical Research Coordinator B/C (Department of Radiology) Job...and help to manage correspondence with sponsor & regulatory review boards. Coordinator B: A Bachelor's Degree,… more
- University of Rochester (Rochester, NY)
- …and consent form development, budget development, negotiation and implementation, discussions with the human subjects review board and the University's legal ... Organize and plan project start up, including applying for IRB , GCRC, and IBC approvals. Prepare documents for regulatory...combination of education and experience required. + Experience as Human Subject Research Coordinator I… more
- University of Washington (Seattle, WA)
- …a license/certification/registration.** **ADDITTONAL REQUIREMENTS** + Demonstrated experience as a research coordinator for both investigator-initiated human ... prior research or training experience to include oversight of coordinator activities within the division including IRB submissions, the maintenance… more
- University of Pennsylvania (Philadelphia, PA)
- … B will assist the regulatory specialist in preparing for all local and Central Institutional Review Board ( IRB ) documentation through the IRB ... and Human Genetics) Job Profile Title Clinical Research Coordinator A Job Description Summary The...regulatory specialist in preparing for all local and Central Institutional Review Board ( IRB… more
- University of Pennsylvania (Philadelphia, PA)
- …as part of a team, as well as independently; knowledge of IRB and human research protection regulations. Coordinator B: Bachelor's degree and 2-4 years ... home for work and play. Posted Job Title Clinical Research Coordinator - Temporary Job Profile Title Temporary...or CRO- including source documentation, case report forms, and research charts. Collect, review and report study… more
- University of Rochester (Rochester, NY)
- …research data. **Regulatory:** Coordinates and monitors study processes and study data for institutional review board ( IRB ) submissions and reporting, ... required + or equivalent combination of education and experience required + Experience as Human Subject Research Coordinator 1 preferred + Word processing… more
- GAP Solutions Inc (Baltimore, MD)
- …regulatory documentation for Institutional Review Board ( IRB ). + Participate in developing and maintaining research protocol documentation and ... Objective: Provide services as a Community Brain Health Study Research Coordinator in support of the overall... Institutional Review Board ( IRB ). + Develop and maintain research protocol… more