- 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
- Trinity Health (Syracuse, NY)
- **Employment Type:** Full time **Shift:** Day Shift **Description:** ** Institutional Review Board Specialist - St. Joseph's and St. Peter's Health Systems** ... Summary** : Responsible for coordinating the operations of SJH/SPHP ( IRB ), the IRB Coordinator is...matters pertaining to protecting the rights and welfare of human research participants. + Ensures that submitted… 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
- 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)
- …met before enrollment. + 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
- Nuvance Health (Poughkeepsie, NY)
- … patient, protocol implementation, data collection and query resolution, and submission to the Institutional Review Board ( IRB ). Coordinates studies in ... *Description* *Clinical Research Coordinator - Poughkeepsie, NY* *40...protocols, consent forms, and other required documents to the Institutional Review Board ( IRB… more
- Mount Sinai Health System (New York, NY)
- …study information. Assists in preparing grant applications and documents (for eg, Institutional Review Board , Grants and Contracts Office). ... **Job Description** The Clinical Research Coordinator assists in the daily...research experience Non-Bargaining Unit, 857 - Rehabilitation and Human Performance - ISM, Icahn School of Medicine, Rehab… more
- Mount Sinai Health System (New York, NY)
- …and proposals by developing pilot studies and generating pre-clinical data. + Completes all Institutional Review Board ( IRB ) or IACUC and other ... **Job Description** The Research Program Coordinator I develops and/or...final reports from study. This position is responsible for human subjects or laboratory research , depending on… more
- Actalent (Syracuse, NY)
- Job Description We are seeking a dedicated Clinical Research Coordinator to join our dynamic research team. The successful candidate will manage multiple ... research trials, including first-in- human through phase 3 trials, ensuring compliance with FDA...maintain regulatory documents. + Prepare Informed Consent Documents with institutional language. + Interface with the IRB ,… more
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