• Associate Director - Clinical Operations

    Lilly (Boston, MA)
    …to the development and review of key regulatory documents (eg, Protocol , Investigator Brochure, Clinical Study Report, Informed Consent Forms, patient-facing ... materials, and vendor plans). + Assist in maintaining a quality-focused clinical infrastructure by developing, revising, and implementing SOPs to ensure operational consistency with GXP standards across trials and programs. + Engage in the planning of quality… more
    Lilly (10/31/25)
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  • Assistant/ Associate Research Professor…

    University of Virginia (Charlottesville, VA)
    …to negotiate, influence, and consult on a wide range of projects, protocol standards, effective and efficient research processing, and study techniques and ... standards. This position is expected to be a leader within the research team and communicate with the department leadership research findings, new available research, and designs and techniques that will improve data functionality, research methodologies, and… more
    University of Virginia (10/31/25)
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  • Principal Faculty - Assistant/ Associate

    Franklin Pierce University (Round Rock, TX)
    …in university activities. + Meet requirements articulated in the faculty protocol . + Other duties as assigned. Position Requirements/Skills/Abilities: + Must have ... knowledge of educational, management, and adult learning theory and principles and be able to administer, assess, and document programmatic education trends and data. + Must have a minimum of 3 years of clinical experience as a practicing provider. + Previous… more
    Franklin Pierce University (10/24/25)
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  • Clinical Research Associate 1

    SUNY Upstate Medical University (Syracuse, NY)
    …sponsor/CRO regulatory correspondence. Communication with IRBs, sponsors, and protocol -related Upstate Departments. Pre-screen, Screen, and enroll research ... participants in outpatient ALS clinical trials. Additional duties include but are not limited to: process and ship lab samples, schedule and conduct follow up research appointments for clinical trial participants, data collection and entry into paper and… more
    SUNY Upstate Medical University (10/16/25)
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  • Mental Health Associate - Community…

    Carle Health (Peoria, IL)
    …knowledge base of advanced directives Administers/scores assessment scales per protocol Participates in interdisciplinary clinical staffing's or ensures pertinent ... information is provided to team Develops, reviews, and revises plan of care on assigned patients Completes required documentation as appropriate including assessment scales Addresses the patient's strengths, impairments and interventions identified in the plan… more
    Carle Health (10/14/25)
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  • Research Associate - QC Stem Cell

    Bio-Techne (Minneapolis, MN)
    …Performing routine quality control testing of stem cell products using protocol -defined assays to demonstrate their activity. The assays include culturing and ... handling of stem cells, primary cells, and basic cell lines for use in flow cytometry and immunocytochemistry (ICC). The position requires routine documentation, data analysis and good communication of results. Good Manufacturing Practice (GMP) documentation… more
    Bio-Techne (10/07/25)
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  • Associate Engineer, Control Systems…

    Allison Transmission (Indianapolis, IN)
    …Programming experience in Microsoft Visual Studio C/C++ + Vehicle communication protocol development experience - CAN/J1939, PTCAN, GMLAN, UDS, OBD2, etc. Preferred ... Experience: + Experience in MATLAB/Simulink system modelling software + Experience in transmission/powertrain/vehicle system modelling + Experience with HIL and/or SIL simulation methods + Experience with Veristand and LabView + Experience with GitHub for… more
    Allison Transmission (10/01/25)
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  • Research Associate - QC Bioassay

    Bio-Techne (Minneapolis, MN)
    …a variety of laboratory techniques. This position is responsible for performing protocol -defined bioassays on proteins and antibodies to demonstrate the activity of ... a product. The position requires maintenance of cell lines and isolation of primary cells for use in the assays. Good Manufacturing Practice (GMP) documentation and workflow is required in this position. **ESSENTIAL FUNCTIONS** + Maintain cell lines; isolate… more
    Bio-Techne (09/27/25)
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  • Clinical Trials - Clinical Data Associate

    Lilly (Indianapolis, IN)
    …database design, and observed dataset requirements are reflective of specific protocol objectives + Specifies the data collection tools and technology platforms ... for the trial/program + Drive standards decisions, implementation and compliance for the study/program + Help create scope scenarios and negotiate outcomes with study teams while taking into account the cost and value of scenarios + Facilitate/assimilate… more
    Lilly (09/25/25)
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  • Research Associate

    North Carolina Agriculture & Technical State Unive (Greensboro, NC)
    …plan and design specific quality control measures and procedures as part of research protocol . * Ability to define standards for the collection of data; ability to ... set standards for accuracy, validity and integrity; ability to lead others in analysis. * Ability to adapt experimental design based upon interpretation of data and or literature review, in collaboration with others. * Ability to co-author/ author manuscripts… more
    North Carolina Agriculture & Technical State Unive (09/24/25)
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