- University of Texas Rio Grande Valley (Mcallen, TX)
- …and welfare in compliance with Institutional Review Board ( IRB ) regulations for the Human Subjects Protections Program. Description of Duties + ... Human Subjects Protections Program and communicates with the Institutional Review Board regarding the...of experience conducting IRB reviews or conducting human subjects' research in a regulated environmentorMaster's… 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
- University of Rochester (Rochester, NY)
- …the individual, and internal equity considerations._ **Responsibilities:** GENERAL SUMMARY The Human Subject Coordinator (HSRC) Trainee will assist with ... the Adolescent Brain and Cognitive Development (ABCD) Study, a federally funded research study in the Cognitive Neurophysiology Lab. General protocol and directions… more
- General Dynamics Information Technology (Portsmouth, VA)
- …Portsmouth (NMCP). The CRC is responsible for providing research coordination support for IRB - and IACUC -approved human and animal research protocols in ... entity may be required for safety reasons. + Coordinate research activities of assigned IRB and IACUC-approved...leadership skills as the coordinator of complex human and animal research protocols. + Maintain… 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)
- …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
- MetroHealth (Cleveland, OH)
- … coordinator working with human subjects. Experience working with an Institutional Review Board ( IRB ). Good organizational and problem-solving ... or other related field. Three years of experience working as a clinical research coordinator working with human subjects, or two years of experience and… 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)
- …+ 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
- 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). **_The grant ... **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
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