• Clinical Research Regulatory

    University of Rochester (Rochester, NY)
    GENERAL PURPOSE: The Clinical Research Regulatory Coordinator II is responsible, for the coordination and oversight of regulatory requirements of ... with the Principal Investigator (PI) and other study team members, the Clinical Research Regulatory Coordinator II exhibits increased learned skills… more
    University of Rochester (06/06/24)
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  • Clin Research Reg Spt Spec I

    University of Rochester (Rochester, NY)
    GENERAL PURPOSE: The Clinical Research Regulatory Coordinator I is an entry level position, responsible, under close supervision, for the coordination ... with the Principal Investigator (PI) and other study team members, the Clinical Research Regulatory Coordinator I exhibits increased learned skills… more
    University of Rochester (06/13/24)
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  • Clinical Research Coordinator

    University of Rochester (Rochester, NY)
    GENERAL PURPOSE: The Clinical Research Coordinator III (CRC III) is an experienced Clinical Research Professional responsible for providing ... research protocols/procedures preferred. + Proficiency in medical terminology, the clinical research process and applicable regulatory guidelines,… more
    University of Rochester (06/15/24)
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  • Human Subject Research Coordinator

    University of Rochester (Rochester, NY)
    …as appropriate. Maintains current CITI credentials for Human Subject Protection, GCP, Clinical Research Coordinator , plus additional sponsor GCP ... Investigator at study meetings as needed. (10%) Manages the regulatory details for assigned research studies. Prepares...Attends training sessions and other educational opportunities related to clinical research in order to keep current… more
    University of Rochester (06/30/24)
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  • Human Subject Research Coordinator

    University of Rochester (Rochester, NY)
    …coordination; or equivalent combination of education and experience preferred. + Certified Clinical Research Coordinator and/or nursing degree preferred. ... in Pediatric Infectious Diseases to conduct surveillance studies and clinical trials. In particular, this individual will be responsible...needed + Interact with Project Coordinator and Research Lab Director to ensure regulatory and… more
    University of Rochester (04/25/24)
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  • Human Subject Research Coordinator I

    University of Rochester (Rochester, NY)
    …Lab at the University of Rochester is searching for a full-time Human Subjects Research Coordinator who will contribute to a federally funded investigation of ... to get our lab members actively involved in ongoing research projects. The University of Rochester is considered a...+ Collaborates with Professors Keane and Poletti to ensure regulatory and other documents (eg, NIH progress reports) are… more
    University of Rochester (06/30/24)
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  • Human Subject Res Coordinator II,…

    University of Rochester (Rochester, NY)
    …the sponsor's team, including the Project Manager, to resolve queries from clinical research visits. Interfaces with collaborating investigators, sponsors, and ... combination of education and relevant experience required. + Experience as Human Subject Research Coordinator I preferred + Knowledge of word processing and data… more
    University of Rochester (06/30/24)
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  • Clinical Research Spec II

    University of Rochester (Rochester, NY)
    GENERAL PURPOSE: The Clinical Research Coordinator II (CRC II) is a mid-level Clinical Research Professional responsible for assisting in the ... planning, coordinating, implementing, monitoring, and evaluating specific clinical research studies as assigned. Under the ultimate responsibility of the… more
    University of Rochester (06/13/24)
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  • Clinical Research Spec II

    University of Rochester (Rochester, NY)
    … coordination; or equivalent combination of education and experience required. + Clinical Research Coordinator experience and/or nursing degree preferred. ... and conference calls as needed. + Interact with Project Coordinator and Research Lab Director to ensure regulatory and other documents are complete and… more
    University of Rochester (06/30/24)
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  • CTCC Coordinator

    University of Rochester (Rochester, NY)
    …eg an Associate's degree and completion of 6 months in the Human Subject Research Coordinator Trainee program preferred. + 2 years' experience in clinical ... technology-related research studies. May assist Principal Investigator in conducting clinical studies, and in presenting study research results. Interacts… more
    University of Rochester (06/30/24)
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  • Department Coordinator IV

    University of Rochester (Rochester, NY)
    Coordinator is the central liaison and support person for all non- clinical activities in the Division. The Department Coordinator is responsible for ... revenue, and operational expenses. Completes and processes University forms for clinical and research expenses across divisions, including but not limited… more
    University of Rochester (06/08/24)
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  • Neurology Study Coordinator - CRNG

    University of Rochester (Rochester, NY)
    …accordance with Good Clinical Practice standards and guidelines. Manages the regulatory details for assigned research studies. Prepares and maintains ... POSITION SUMMARY: Coordinates all aspects of assigned research studies associated with human subject research...amendments and continuing reviews for IRB approval. Ensures all regulatory requirements are met and documented. (10%) + Acts… more
    University of Rochester (06/30/24)
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  • Sr Human Subject Research Spec

    University of Rochester (Rochester, NY)
    …for independent judgement, this individual will have the responsibility for managing clinical research trials, from industry, NIH, foundations and internal ... will oversee the day to day operations of the clinical research , support personnel as well as...consent and/or collect specimens/samples. **RESPONSIBILITIES:** + Perform Human Subject Research Coordinator duties as needed and those… more
    University of Rochester (06/11/24)
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  • Human Sub Research Spec II

    University of Rochester (Rochester, NY)
    GENERAL PURPOSE: Human Subject Research Specialist II is a mid-level clinical research coordinator responsible for assisting in the planning, ... in UR-specific research software needed to manage clinical research protocols Other duties as assigned...Word processing and data analysis software reuqired. + Professional Research Coordinator certification (SoCRA or ACRP) preferred.… more
    University of Rochester (04/26/24)
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  • Human Subject Research Coord II

    University of Rochester (Rochester, NY)
    …Human Subject Research Coordinator I preferred + Certified Clinical Research Coordinator and/or nursing degree desirable/preferred. Phlebotomy ... GENERAL PURPOSE: The part-time research coordinator (20hrs/wk flexible schedule to...contacts and relationships between and among Principal Investigator (PI), research staff, study sites and sponsoring and regulatory more
    University of Rochester (06/30/24)
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  • Human Subject Research Spec I

    University of Rochester (Rochester, NY)
    …PURPOSE: Human Subject Research Specialist I is an entry level clinical research coordinator responsible for coordinating the activities associated ... study. This role will assume responsibility for less complex clinical research protocols, receiving guidance and instruction...and completion of 6 months in the Human Subject Research Coordinator Trainee program) required. + Word… more
    University of Rochester (06/30/24)
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  • Human Sub Research Spec II

    University of Rochester (Rochester, NY)
    …has a robust research portfolio that encompasses basic, translational, and clinical research . This individual would support Clinical Trials under ... UR-specific research software, such as ClickIRB and OnCore, needed to manage clinical research . + Assumes personal responsibility for keeping up with new… more
    University of Rochester (06/30/24)
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  • Clin Research Reg Spt Spec II

    University of Rochester (Rochester, NY)
    …participating in any research -related procedures. + Minimum of 3 years of clinical research or equivalent combination of education and experience required. + ... contacts and relationships between and among Principal Investigator (PI), research staff, study sites and sponsoring and regulatory...Experience as Human Subject Research Coordinator I preferred. + Word processing… more
    University of Rochester (05/28/24)
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  • NCORP Research Project Manager - DiRECT

    University of Rochester (Rochester, NY)
    …the URCC NCORP Research Base. This position serves as liaison between the Research Base and clinical research personnel at off-site locations, including ... physicians, nurses, study coordinators, and clinic staff, in all phases of assigned clinical research protocols. Working collaboratively with the PI, other NCORP… more
    University of Rochester (05/09/24)
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  • OT Clinical Therapist

    University of Rochester (Rochester, NY)
    …appropriate corrective action when inconsistency of activities is identified. 10% + Trains clinical research coordinator and other staff on activities ... OT Clinical Therapist is responsible for performing clinical research activities to include, but not...the contacts and relationships between and among the URNI, research staff, study sites and sponsoring and regulatory more
    University of Rochester (06/30/24)
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