• Clinical Research Physician - Incretins

    Lilly (Indianapolis, IN)
    …product development activities over the entire spectrum of drug development and clinical trial phases. Specific activities include developing or contributing to ... of phase 3b/4 studies **,** as well as non clinical trial solutions/activities that are conducted in...scientific information needs of all investigators and personnel. + Monitor patient safety during the conduct of studies and… more
    Lilly (07/10/25)
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  • Cancer Clinical Research Coordinator 2…

    Stanford University (Stanford, CA)
    …_Other_ _duties_ _may_ _also_ _be_ _assigned._ **DESIRED QUALIFICATIONS:** + Oncology clinical trial coordination experience. + Investigator Initiated ... Develop and manage systems to organize, collect, report, and monitor data collection. Extract, analyze, and interpret data. +...clinical trial coordination experience. **EDUCATION & EXPERIENCE (REQUIRED):** Bachelor's degree… more
    Stanford University (09/09/25)
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  • Centralized Monitor Technician Cohort (ECG)…

    BJC HealthCare (St. Louis, MO)
    …Cardiac Monitoring, Cardiac Diagnostics Assistant, Cardiology, EMR/EHR, IT Healthcare, Research Clinical Trial Assistant, Unit Clerks, Patient Registrars, ER, ... Centralized Telemetry Monitor Technician (CTMT), Non-patient-facing, non- clinical , ECG Monitor Technicians, patient safety_ **Next Steps:** **If selected to… more
    BJC HealthCare (08/31/25)
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  • Clinical Project Manager

    IQVIA (Durham, NC)
    Job Overview Project Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients' lives by bringing new drugs to ... achievement and to manage study issues and obstacles. * Monitor progress against contract and prepare/present project and/or sub-team...Knowledge of clinical trials - Knowledge of clinical trial conduct, and skill in applying… more
    IQVIA (09/16/25)
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  • Clinical Scientist, Hematology

    Bristol Myers Squibb (Madison, NJ)
    …Summary / Objective** + Will be responsible for design and execution of assigned clinical trial activities and work closely with clinical team members ... activities associated with the conduct + May serve as Clinical Trial Lead for one or more...present these at SIVs and Investigator meetings + Review clinical narratives + Monitor clinical more
    Bristol Myers Squibb (09/14/25)
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  • Director, Clinical Development…

    Gilead Sciences, Inc. (Foster City, CA)
    …therapeutic area, you will lead or support multiple components of clinical trial programs, including primary biliary cholangitis (PBC) and/or ... Foster City, CA. **EXAMPLE RESPONSIBILITIES:** + Lead or support clinical trial protocol design, clinical ...response to health authority inquiries + Serve as medical monitor for clinical trials or oversee medical… more
    Gilead Sciences, Inc. (08/27/25)
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  • Clinical Research Physician - Development

    Lilly (Indianapolis, IN)
    …external health care professionals according to guidelines above. + Participate in reporting of clinical trial data in Clinical Trial Registry ... and clinical data relevant to the molecule. Clinical Research/ Trial Execution and Support + Plans,...scientific information needs of all investigators and personnel. + Monitor patient safety during the conduct of studies and… more
    Lilly (07/25/25)
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  • Lead Clinical Risk Management Analyst

    Abbott (Alameda, CA)
    …are imperfect yet meet the business need. + Proficient in the translation of clinical trial requirements to the technical specifications. + Skilled at making ... medicines. Our 114,000 colleagues serve people in more than 160 countries. **Lead Clinical Risk Management Analyst** **Working at Abbott** At Abbott, you can do work… more
    Abbott (07/19/25)
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  • Medical Director, Clinical Development…

    Ascendis Pharma (Palo Alto, CA)
    …+ Provide leadership to study teams + Ensure successful completion of trial -related documents (including clinical trial protocols, investigator brochures, ... site and subject retention + Serve as a Medical Monitor for clinical trials, ensure study integrity,...position. + At least 3 years of experience with clinical trial design and execution + Strong… more
    Ascendis Pharma (07/04/25)
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  • Data Coordinator - Clinical Research

    Insight Global (Cascade, MI)
    …setting Strong written and verbal communication Detail oriented Hands-on experience with clinical trial software (eg, CTMS, EDC systems, Oncore) Strong ... questions, concerns, as well as status of the protocol. Monitor the overall day-to-day conduct of assigned studies in...understanding of GCP, clinical trial protocols, and regulatory compliance Prior… more
    Insight Global (09/09/25)
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