• Daiichi Sankyo, Inc. (Bernards, NJ)
    …product safety requirements for inclusion in Clinical study protocols (CSPs) and Informed Consent Forms (ICFs), for assigned product(s)Authors or oversees the ... development of the Safety Management Plan for assigned product(s)Independently evaluates safety data of any source to identify potential safety signals and performs safety analysis/evaluation. May contribute to safety action recommendations, and communication… more
    HireLifeScience (10/18/24)
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  • Associate Director , Informed

    Bristol Myers Squibb (Madison, NJ)
    …leveraging internal and external best practices and exploring technologies. The Associate Director (AD), Informed Consent Management role reports to the ... Director of Informed Consent Management. The AD will be responsible for informed consent activities and will also serve as the Global Process Lead for… more
    Bristol Myers Squibb (09/21/24)
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  • Associate Director , Clinical Safety…

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …core product safety requirements for inclusion in Clinical study protocols (CSPs) and Informed Consent Forms (ICFs), for assigned product(s) + Authors or ... oversees the development of the Safety Management Plan for assigned product(s) + Independently evaluates safety data of any source to identify potential safety signals and performs safety analysis/evaluation. May contribute to safety action recommendations,… more
    Daiichi Sankyo Inc. (10/19/24)
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  • Director , Medical Monitor (MD), VRD

    Pfizer (Pearl River, NY)
    …fit with the clinical program strategy. + Ensure that documents (protocol, Informed Consent Document [ICD], etc.) meet regulatory requirements and company ... Provides protocol specific training to study team, investigators, clinical research associate , and others. + Interacts with healthcare professionals at sites… more
    Pfizer (10/31/24)
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  • Executive Director , Global Clinical Lead

    Pfizer (Pearl River, NY)
    …clinical program strategy. + Provides oversight to ensure that documents (protocol, Informed Consent Document [ICD], etc.) meet regulatory requirements and ... + Supports Program specific training to study team, investigators, clinical research associate , and others. + Oversees interactions of clinical team with healthcare… more
    Pfizer (10/10/24)
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  • Per Diem Physician Associate -EHC-13001-023

    Mount Sinai Health System (Elmhurst, NY)
    …pursuant to clinical responsibility, such as arranging follow-up for patients, obtaining informed consent from patients for procedures, recalling patients for ... required professionally or at the request of the supervising physician(s), Director of Service, and/or Supervising Physician Assistant. *-indicates duty is… more
    Mount Sinai Health System (08/16/24)
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  • Per Diem Physician Associate - QHC/Day…

    Mount Sinai Health System (Jamaica, NY)
    …to clinical responsibility, such as arranging follow-up for patients, obtaining informed consent from patients, recalling patients for further evaluation ... required professionally or at the request of the supervising Attending Physician, the Director of Service, and/or Chief Physician Assistant. -The PA may perform the… more
    Mount Sinai Health System (09/28/24)
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  • Clinical Program Manager (RN/NP Required) - Tisch…

    Mount Sinai Health System (New York, NY)
    …Myeloma (MM) Program at Mount Sinai hospital. In collaboration with the MM Medical Director , the Associate Director , and the clinical trials investigators; ... of the research program. The Clinical Program Manager will report into Associate Director . **Qualifications** Education: + Bachelor's Degree (BSN) (required) or… more
    Mount Sinai Health System (08/15/24)
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