- University of Rochester (Rochester, NY)
- …and internal equity considerations._ **Responsibilities:** Coordinates the activities associated with human subject research . **SCHEDULE:** + 8 AM-5 PM; OCC ... + Under the direction of the Principal Investigator, assists in the conduct of research studies beginning with the preparation of IRB materials through the… 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 ... internal equity considerations._ **Responsibilities:** Coordinates the activities associated with human subject research . RESPONSIBILITIES: - Coordinates the… more
- UTMB Health (Galveston, TX)
- …**Preferred** *ACRP or SOCRA Certification *Bilingual (Spanish) **Job Description:** The Clinical Research Coordinator obtains human subject data for ... administrative duties supporting the study. **Job Duties:** + Obtain human subject data for clinical research activities... IRB , OCR or OSP under direction of research coordinator under the direction of the… more
- University of Rochester (Rochester, NY)
- …with study families, and document adverse events and report to senior study staff, PI, Institutional Review Board ( IRB ), Sponsor, and/or any other ... ensures consent forms are complete, accurate, and available for review . Prepares documents for data uploads to NIMH Data...associate's degree and completion of 6 months in the Human Subject Research Coordinator Trainee… 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)
- …works as an integral part of the research team. This role mentors Human Subject Research Coordinator I(s) and supervises students as assigned. ... institutional regulations, policies, and practices related to human subject research . + Serves as the...combination of education and experience preferred. + Experience as Human Subject Research Coordinator I… 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 ... institutional regulations, policies and practices related to human subject research . Develops, implements and evaluates...combination of education and experience required. - Experience as Human Subject Research Coordinator I… more
- University of Rochester (Rochester, NY)
- … Coordinator Certification (ie, SoCRA or ACRP) preferred. + Experience as Human Subject Research Coordinator II preferred. The University of Rochester ... lead at the senior professional level. Manages communication and shared activities for human subject research studies involving units within and external to the… more
- University of Rochester (Rochester, NY)
- …social or technical field or Associate's degree and completion of 6 months in the Human Subject Research Coordinator Trainee Program required + Or an ... considerations._ **Responsibilities:** GENERAL PURPOSE: Coordinates the activities associated with human subject research . **JOB SUMMARY:** **Position Summary**… more
- University of Rochester (Rochester, NY)
- …degree, or required. + Associate's degree and completion of 6 months in the Human Subject Research Coordinator Trainee program, + Equivalent combination of ... **Responsibilities:** GENERAL PURPOSE: We are in search of a human subject research specialist to help support... IRB + Maintains eligibility to participate in research involving human subjects including completing all… more
- University of Rochester (Rochester, NY)
- …+ Bachelor's degree or Associate's degree and completion of 6 months in the Human Subject Research Coordinator Trainee Program + Or an equivalent ... of the individual, and internal equity considerations._ **Responsibilities:** GENERAL PURPOSE The Human Subject Research Specialist I (HSRS I) plays a vital… more
- University of Rochester (Rochester, NY)
- …order to identify potential study candidates. + Work in collaboration with the internal review board ( IRB ) in gaining approval and modifying studies. ... events and bring to the PI's attention and/or the IRB or sponsor as required, and to ensure that...Associate's degree and completion of 6 months in the Human Subject Research Coordinator Trainee… 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
- 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. 3. Assists in the collection, analysis and review of experimental data for publication and presentation. 4.… more
- University of Pennsylvania (Philadelphia, PA)
- …work as part of a team, as well as independently; knowledge of IRB and human research protection regulations. Coordinator A: Bachelor of Science and 1 to ... and resources, and much more. Posted Job Title Clinical Research Coordinator A/B Job Profile Title Clinical...or CRO, includes source documentation, case report forms, and research charts. Collect, review , and report study… more
- University of Pennsylvania (Philadelphia, PA)
- …in the field of lipoprotein metabolism, atherosclerosis, and cardiovascular disease. Assist with Institutional Review Board ( IRB ) filings and inquiries, ... much more. Posted Job Title Clinical Research Coordinator A/B (Department of Translational Medicine and Human...of a team, as well as independently; knowledge of IRB and human research protection… more
- University of Pennsylvania (Philadelphia, PA)
- …biological samples and related study documents, and collection of clinical data. Assist with Institutional Review Board ( IRB ) filings and inquiries, and ... and resources, and much more. Posted Job Title Clinical Research Coordinator A/B (Division of Urology/Department of...AEs, SAEs, and UADEs reports to the Investigator and Institutional Review Board ( IRB… more
- University of Pennsylvania (Philadelphia, PA)
- …biological samples and related study documents, and collection of clinical data. Assist with Institutional Review Board ( IRB ) filings and inquiries, and ... and resources, and much more. Posted Job Title Clinical Research Coordinator A/B ( Department of Medicine...of a team, as well as independently; knowledge of IRB and human research protection… more
- Tufts Medicine (Lowell, MA)
- …staff, ensuring protocol adherence, regulatory compliance, data collection, and communication with the Institutional Review Board ( IRB ). Success in this ... requirements 5. IATA Hazardous Good Shipping Certification 6. CITI Human Research Protection Certification **Duties and Responsibilities:**...reporting any to the (PI), the study sponsor and Institutional Review Board . 8. Reviews… more