• Director, Supplier Relationship Management (Global…

    Takeda Pharmaceuticals (Boston, MA)
    …across key clinical operational functions (eg project management, clinical monitoring, data management process, regulatory affairs, pharmacovigilance, etc.) ... categories: CRO , central and specialty labs, functional service providers, clinical technologies. **This position is currently classified as "hybrid" by Takeda's… more
    Takeda Pharmaceuticals (07/30/25)
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  • Associate Director, Data Sciences, Safety,…

    IQVIA (Durham, NC)
    …+ Operational exposure or experience in any of the following Clinical Data Management, Biostatistics, Statistical Programming, Medical Writing, Lifecycle ... **Associate Director, Data Sciences, Safety, and Regulatory FSP Sales** Associate...General knowledge of the Clinical Development space, Clinical Research Organization ( CRO ) operations, are required.… more
    IQVIA (07/02/25)
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  • Associate Director, Statistics, Medical & Real…

    Otsuka America Pharmaceutical Inc. (Boise, ID)
    …for a strong Clinical Statistician in the Medical and Real World Data Analytics organization to provide statistical expertise for analysis of clinical trials ... assessing economic value, supporting health technology assessments through statistical analyses of clinical and other data . The role will manage the timely… more
    Otsuka America Pharmaceutical Inc. (09/05/25)
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  • Clinical Research Associate 1

    SUNY Upstate Medical University (Syracuse, NY)
    …and ship lab samples, schedule and conduct follow up research appointments for clinical trial participants, data collection and entry into paper and electronic ... Job Summary: The Clinical Research Associate I will be responsible for...limited to: performance of regulatory tasks including IRB and sponsor/ CRO regulatory correspondence, communication with IRBs, sponsors, and protocol-related… more
    SUNY Upstate Medical University (08/29/25)
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  • Clinical Research Associate 1

    SUNY Upstate Medical University (Syracuse, NY)
    …and ship lab samples. Schedule and conduct follow up research appointments for clinical trial participants. Data collection and entry into paper and electronic ... Job Summary: Coordination of clinical research studies. Performance of regulatory tasks including IRB and sponsor/ CRO regulatory correspondence. Communication… more
    SUNY Upstate Medical University (08/21/25)
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  • Global Clinical Pathology Scientist

    Pfizer (Groton, CT)
    …RESPONSIBILITIES** + Generates and ensures the delivery of the highest quality of Clinical Pathology/ Biomarker study data for both internal DSRD/RU and external ... multi-site studies. + Reviews and evaluates Hematology, Coagulation, Clinical Chemistry, Urinalysis and Immunoassay data , processes and analyzes study samples… more
    Pfizer (07/31/25)
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  • Clinical Lead, Early Clinical…

    Sanofi Group (Morristown, NJ)
    …& Decision Science), Early Development Clinical Operations (EDCO, including Clinical Trial Managers and Data Managers), Regulatory Affairs, Patients Safety ... & Decision Science), Early Development Clinical Operations (EDCO, including Clinical Trial Managers and Data Managers), Regulatory Affairs, Patients Safety… more
    Sanofi Group (07/29/25)
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  • FSP Principal Biostatistician- Early Phase…

    IQVIA (Durham, NC)
    …including timelines, deliverables, and availability of resources. + Collaborate with Data Management, Clinical Development, and Clinical Pharmacologists/PK ... Level:** FSP Senior or Principal Biostatistician for Early Phase Clinical Development (PK) **Location:** Home-based in the US or...**Location:** Home-based in the US or Canada **Why DSSS?** Data Sciences Staffing Solutions, DS3, is a unit within… more
    IQVIA (07/15/25)
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  • Sr. Director, Global Clinical Operations TA…

    Teva Pharmaceuticals (West Chester, PA)
    …ICH guidelines and clinical operations + Proven experience in vendor and CRO management + Proven experience in process improvement and design, as well as project ... thinking + Strong presentation and communication skills + Extensive knowledge in clinical trials methodology **Compensation Data ** The annual starting salary for… more
    Teva Pharmaceuticals (07/17/25)
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  • Associate Director, Feasibility

    Takeda Pharmaceuticals (Boston, MA)
    …execution and patient enrollment. + Strong analytical competencies. Exposure to and understanding of clinical data sets as it relates to clinical trial ... data -driven feasibility assessments for Phase I - IV clinical studies, including protocol design optimization, country/site identification, enrollment strategy… more
    Takeda Pharmaceuticals (08/27/25)
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