• Sr. Clinical Research Associate - Oncology - TX…

    Parexel (Albany, NY)
    …accordance with applicable prevailing laws, Good Clinical Practices (GCP), and the Sponsor 's standards. The Sr. CRA is accountable for site management and ... the Study Monitoring Plan (SMP) and applicable prevailing laws, GCP, and the Sponsor 's standards to achieve project goals, timelines and quality + Manage assigned… more
    Parexel (12/11/25)
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  • *Hybrid* Accounts Receivable Analyst (R25-57)

    The Research Foundation for SUNY at the University at Albany (Albany, NY)
    …Prepare and submit accurate billings and financial status reports in sponsor -specific formats. + Review grant/contract documentation to ensure proper categorization ... payment issues. + Manage award closeouts, cash transfers and sponsor refunds. + Stay current with sponsor ,...and sponsor refunds. + Stay current with sponsor , federal, and state regulations. + Build positive relationships… more
    The Research Foundation for SUNY at the University at Albany (12/05/25)
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  • Senior Clinical Research Specialist

    University of Rochester (Rochester, NY)
    …from protocol development and initiation to study close-out according to regulatory/ sponsor guidelines, ensures each study's integrity, and mentors less experienced ... external audits. + Effectively communicates with the research team, sponsor , data coordinating centers, compliance monitors, collaborators, investigators, academic… more
    University of Rochester (12/05/25)
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  • Research Coordinator - RN

    University of Rochester (Rochester, NY)
    …national regulations, Good Clinical Practice (GCP) guidelines, institutional policies, and sponsor protocols. This role supports Phase I-III clinical trials and ... study material management. Training & Professional Development - 5% + Sponsor training, GCP certification, and continuing education. **Clinical Research Operations**… more
    University of Rochester (12/05/25)
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  • Clinical Research Spec II

    University of Rochester (Rochester, NY)
    …coordination duties from protocol initiation to study close-out according to regulatory/ sponsor guidelines. Assists in assuring the overall integrity of studies. ... external audits. + Effectively communicates with the research team, sponsor , data coordinating centers, compliance monitors, collaborators, investigators, academic,… more
    University of Rochester (11/25/25)
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  • Senior Program Administrator - CIMS

    Rochester Institute of Technology (Rochester, NY)
    …the marketing coordinator to ensure messaging accurately represents GIS/CIMS and its sponsor (s) and complies with contract requirements. + Work with the program ... regard to scope, schedule, and budget, as well as compliance with RIT, GIS, and sponsor requirements. + Use critical thinking skills in the creation of and review of… more
    Rochester Institute of Technology (11/19/25)
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  • Sr Human Subject Research Spec

    University of Rochester (Rochester, NY)
    …interacting with research participants. May provide training on federal, state, sponsor and/or institutional regulations, policies and practices related to human ... and generally in compliance with Good Clinical Practice (GCPs) guidelines and sponsor requirements. Directs the activities of subordinate staff and relevant others… more
    University of Rochester (11/06/25)
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  • Principal Quantitative Clinical Pharmacologist…

    Cytel (Albany, NY)
    …to what it could be. You motivate others to do the same. ** Sponsor -dedicated:** Working fully embedded within one of our pharmaceutical clients, with the support ... regulatory authorities. + Develop strong collaboration and communication with sponsor cross-functional teams and sponsor Biostatistics management. **Required**… more
    Cytel (10/30/25)
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  • Human Subject Research Spec II

    University of Rochester (Rochester, NY)
    …site human subject studies. May provide training on federal, state, sponsor and/or institutional regulations, policies and practices related to human subject ... and generally in compliance with Good Clinical Practice (GCPs) guidelines and sponsor requirements. + May direct the activities of subordinate staff and others… more
    University of Rochester (10/23/25)
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  • Clinical Research Data Specialist

    University of Rochester (Rochester, NY)
    …operating procedures. Coordinates with the Principal Investigators (PI), staff, and sponsor -designated contacts to resolve data inquiries as needed. Responsible for ... standard operating procedures (SOPs). + Maintains screening, enrollment, and other sponsor and/or protocol specific logs, as required by protocol and department… more
    University of Rochester (10/23/25)
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