• Development Scientific Director, I&I

    Sanofi Group (Morristown, NJ)
    …management plans to assure successful execution of the clinical trials in compliance with Good Clinical Practice (GCP), applicable laws and regulations as well ... Participate in the elaboration of training material and presentations at the investigator meetings/local teams trainings + Answer to medical questions raised by HA,… more
    Sanofi Group (11/21/25)
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  • Postdoctoral Fellow- Computational Biology

    MD Anderson Cancer Center (Houston, TX)
    …to support the postdoc's transition from mentored research to independent investigator . Research Topics include mathematical and computational modeling of cancer ... to disseminate results to the scientific community, assisting the principal investigator with mentoring junior lab members. Members of the Butner laboratory… more
    MD Anderson Cancer Center (11/20/25)
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  • Clinical Development Lead Prostate (Acp3)

    Bristol Myers Squibb (San Diego, CA)
    …regulatory authority interactions, design and execution of Phase 1 to Phase 3 clinical trials, and medical monitoring. This role works collaboratively with ... to design and implement clinical studies + Contribute to writing of protocols, investigator brochures, clinical study reports, and review of other clinical trial and… more
    Bristol Myers Squibb (11/19/25)
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  • Senior Research Assistant

    Kennedy Krieger Institute (Baltimore, MD)
    …clinical and translational neuroimaging research with supervision from the Principal Investigator (PI). This will include oversight of lab research operations, ... (IRB) applications for clinical projects as well as grant-writing, where appropriate. 3 . Discuss ongoing trials with patients and assist in obtaining informed… more
    Kennedy Krieger Institute (11/19/25)
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  • Clinical Research Data Specialist

    University of Miami (Plantation, FL)
    …standard operating p rocedures , under the supervisio n of the Principal Investigator (PI) and supervisor . The Clinical Research Data Specialist is responsible for ... the compilation, registration and submission of data, monitoring compliance with the protocol, adherence to SOPs, and all...a workload of studies commensurate to level of experience 3 . Answers data clarifications (ie data queries) for each… more
    University of Miami (11/18/25)
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  • Postdoctoral Fellow-MSH

    Mount Sinai Health System (New York, NY)
    …applied to conduct the research. 2. Coordinates project activities to meet deadlines. 3 . Collaborates with the PI in the development of new projects and research ... Operating Procedures (SOPs) specific for each study. 5. Assists the Principal Investigator with publications by extracting and compiling moderate to complex research… more
    Mount Sinai Health System (11/17/25)
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  • Clinical Research Coordinator 2

    University of Miami (Miami, FL)
    …collection/recording, and daily operations of moderate risk clinical research protocols. 3 . Collects, processes, packs, and ships specimens according to protocol, ... standards and clinical credentials as delegated by the Principal Investigator . 6. Monitors, documents, reports, and follows-up on study unanticipated/adverse… more
    University of Miami (11/15/25)
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  • Clinical Research Coordinator 2

    University of Miami (Miami, FL)
    …collection/recording, and daily operations of moderate risk clinical research protocols. 3 . Collects, processes, packs, and ships specimens according to protocol, ... standards and clinical credentials as delegated by the Principal Investigator .6. Monitors, documents, reports, and follows-up on study unanticipated/adverse events… more
    University of Miami (11/11/25)
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  • Clinical Research Coordinator 2 - Clinical…

    University of Miami (Miami, FL)
    …collection/recording, and daily operations of moderate risk clinical research protocols. 3 . Collects, processes, packs, and ships specimens according to protocol, ... standards and clinical credentials as delegated by the Principal Investigator .6. Monitors, documents, reports, and follows-up on study unanticipated/adverse events… more
    University of Miami (11/07/25)
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  • Clinical Research Coordinator 2

    University of Miami (Miami, FL)
    …data collection/recording, and daily operations of moderaterisk clinical research protocols. 3 . Collects, processes, packs, and ships specimens according to protocol, ... practice standards and clinical credentials as delegated bythe Principal Investigator .6. Monitors, documents, reports, and follows-up on study unanticipated/adverse… more
    University of Miami (11/07/25)
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