• Clinical Research Coordinator Associate

    Avispa Technology (Palo Alto, CA)
    …primary contact with research participants, sponsors, and regulatory agencies. Coordinate studies from start-up through close-out. * Determine eligibility of and ... gather consent from study participants according to protocol. Assist in developing recruitment...Manage research project databases, develop flow sheets and other study related documents, and complete study documents/case… more
    Avispa Technology (01/08/26)
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  • Administrative Officer

    Department of State - Agency Wide (Stamford, CT)
    …with production figures, status of projects, and cost of operations. Designs, studies , and develops qualitative and quantitative data in support of management ... hours is equivalent to 1 full-time year of graduate study (your school and department determine what constitutes 1...determine what constitutes 1 full time year of graduate study ). The percentage of specialized work experience and the… more
    Department of State - Agency Wide (01/08/26)
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  • Clinical Team Manager/Sr. (CTM) - FSP

    ThermoFisher Scientific (Greenville, NC)
    …clinical deliverable (usually clean data from evaluable patients as specified in the study protocol) within the time period specified in the contract with the ... moderate to high complexity, and may assume regional lead or Clinical Study Manager responsibilities. **Essential Functions:** + Manages all aspects of monitoring… more
    ThermoFisher Scientific (01/07/26)
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  • Research Supervisor

    Cleveland Clinic (Cleveland, OH)
    …team has the knowledge, guidance, and resources necessary to conduct innovative studies aimed at refining treatments, medical services, and more, helping advance our ... quality and safe patient care, anticipating and resolving patient care and study issues by serving as a liaison between investigators, research personnel, outside… more
    Cleveland Clinic (01/07/26)
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  • Clinical Research Nurse Coordinator

    Arkansas Children's (Little Rock, AR)
    …Information:** The Clinical Research Nurse Coordinator coordinates of clinical research studies . Serves as a resource for research study participants, ... members of the clinical research team regarding specified aspects of the study . The Clinical Research Nurse upholds standards for human subjects protection.… more
    Arkansas Children's (01/07/26)
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  • Sr. Clinical Team Manager (CTM)/ Prin. - Neurology

    ThermoFisher Scientific (Greenville, NC)
    …clinical deliverable (usually clean data from valuable patients as specified in the study protocol) within the time period specified in the contract with the ... **Key responsibilities:** + Manages all clinical operational and quality aspects of allocated studies , of low to moderate complexity, in compliance with ICH GCP. In… more
    ThermoFisher Scientific (01/06/26)
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  • Sr Principal Scientist - Imaging

    Regeneron Pharmaceuticals (Tarrytown, NY)
    …early- and late-phase clinical trials. This role involves collaboration with cross-functional study teams where you will lead the design of complex imaging ... pipeline. + Provide leadership during the strategy phase of study design, guiding the team on all imaging aspects...ensure the delivery of high-quality imaging data in clinical studies . This includes drafting imaging manuals and other documents… more
    Regeneron Pharmaceuticals (01/02/26)
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  • Instructional Systems Specialist

    Naval Education and Training Command (Port Hueneme, CA)
    …equipment, testing, and student counseling. You will conduct research and studies to identify new methodologies, technologies, and techniques to improve the ... to be filled. The course work must have included study in at least four of the following five...five areas: Learning theory, psychology of learning, educational psychology: Study of learning theories as they relate to the… more
    Naval Education and Training Command (12/30/25)
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  • Senior Medical Director, Clinical Research…

    Sumitomo Pharma (Montgomery, AL)
    …Duties and Responsibilities** + Responsible for and lead all activities related to clinical study design from clinical study concept to clinical study ... complex decisions + Leads and drives strategy for clinical studies for assigned asset(s) within the Ophthalmology therapeutic area...reporting + Provide clinical input for and participate in study set up and design including data collection tools,… more
    Sumitomo Pharma (12/27/25)
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  • Clinical Research Coordinator

    System One (Rochester, NY)
    …Responsibilities The clinical Research Coordinator will manage all aspects of a study ensuring adherence to the protocol, GCP, and applicable regulations, including ... participating in the informed consent process, coordinating, and performing all study visit procedures per protocol, managing Investigational Product and study more
    System One (12/26/25)
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