• Donor Recruitment Account Manager

    American Red Cross (Portland, OR)
    …annual goals and provide the highest level of customer service to encourage the sponsor to grow their blood program with the Red Cross in frequency and performance ... metrics. 5. Schedule education programs for blood drive sponsor contact, recruitment committees and volunteers within assigned groups to assist in meeting collection… more
    American Red Cross (12/10/25)
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  • Research Nurse (Oncology) - #Staff

    Johns Hopkins University (Baltimore, MD)
    …& clarifies concerns and questions about new protocols with PI and sponsor . + Reviews prospective reimbursement analysis (PRA) as appropriate. _Pre-initiation_ + As ... consent in medical record. + Registers research subjects per sponsor guidelines. + In conjunction with PI, monitors protocol...event reports and ensures proper and timely distribution to sponsor and IRB. + Grades identified toxicities per NCI… more
    Johns Hopkins University (12/10/25)
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  • Research Protocol Specialist - #Staff

    Johns Hopkins University (Baltimore, MD)
    …tracked, and maintained in compliance with institutional, regulatory, and sponsor requirements. **Specific Duties & Responsibilities** + Coordinate the submission, ... systems or libraries. + Enter study data into required institutional or sponsor registration systems. + Assist with protocol development, consent document drafting,… more
    Johns Hopkins University (12/09/25)
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  • Clinical Research Assistant

    Fresenius Medical Center (Tupelo, MS)
    …are compiled and submitted in a timely manner to the CRO, study sponsor or IRB as applicable. + Assists with maintaining constant communication with Institutional ... data into case report forms. + Assists with addressing and resolving study sponsor questions, concerns, and queries in accordance with timelines established by the… more
    Fresenius Medical Center (12/06/25)
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  • Regulatory Operations Manager - Pediatrics

    Dana-Farber Cancer Institute (Boston, MA)
    …oversight of the day-to-day coordination and overall management of sponsor activities for assigned clinical trials; industry sponsored, multi-center, PI-initiated ... reporting. Ensure various regulatory reporting required are met, Study Sponsor , FDA, IRB etc. + Serve as facilitator for...etc. + Serve as facilitator for study team and sponsor (as needed) regarding study status information, critical safety… more
    Dana-Farber Cancer Institute (12/06/25)
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  • Environmental Educator 2 - NY Helps

    New York State Civil Service (Albany, NY)
    …opportunities *Assisting with monitoring budget needs and spending reports Sponsor Organizations *Managing and strengthening sponsor organization partnerships ... and implementing promotional items to support camper and staff recruitment, sponsor involvement, and special events that support the Camps program *Linking… more
    New York State Civil Service (12/05/25)
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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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  • Head and Neck Clinical Research Coordinator

    University of Colorado (Aurora, CO)
    …of data validity and corrects/revises data as appropriate; responds to queries from Sponsor + Adhere to research regulatory standards + Maintain detailed records of ... standard operating procedures and other regulatory guidelines + Assists with Sponsor , Data Safety Monitoring, and Food and Drug Administration (FDA) audits… more
    University of Colorado (12/05/25)
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