• Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …and immune disorders.Summary This position supports the strategy for driving global Clinical Study Start-Up activities for PV Safety Operations. This position ... and electronic data capture (EDC) Safety report outputs, reviews clinical study protocols and the Clinical... protocols to ensure consistency in safety requirements across studies related to a similar compound. Develops and maintains… more
    HireLifeScience (03/19/24)
    - Save Job - Related Jobs - Block Source
  • Senior Manager , Feasibility

    Takeda Pharmaceuticals (Trenton, NJ)
    …**GOALS:** + Conduct data-driven feasibility assessments for Phase I - IV clinical studies , including protocol design optimization, country/site feasibility and ... and establish a geographic country footprint and proposed sites for participation in a clinical study . + Leverage leading industry tools and data sources to… more
    Takeda Pharmaceuticals (02/24/24)
    - Save Job - Related Jobs - Block Source
  • Myeloma Research Program Manager (Cancer…

    University of Pennsylvania (Philadelphia, PA)
    …budgets, patient visits, transporting specimens, data entry, query resolution and working with study monitors). The Program Manager will work closely with major ... operations of clinical research proposals for their team. The Program Manager will work with Investigators and data informatics teams/programs to ensure the… more
    University of Pennsylvania (04/16/24)
    - Save Job - Related Jobs - Block Source
  • Manager , Feasibility

    Takeda Pharmaceuticals (Trenton, NJ)
    …**GOALS:** + Conduct data-driven feasibility assessments for Phase I - IV clinical studies , including protocol design optimization, country/site feasibility and ... define an optimal geographic country footprint and proposed sites for participation in a clinical study . + Leverage leading industry tools and data sources to… more
    Takeda Pharmaceuticals (02/24/24)
    - Save Job - Related Jobs - Block Source
  • Senior Clinical Research Coordinator

    Vitalief (New Brunswick, NJ)
    …Responsibilities: + Under the direct supervision of the Nurse Manager of Clinical Research Center, performs patient ... Participates in site preparation for trials including protocol feasibility, preliminary study budget, startup meeting preparation, training staff, and… more
    Vitalief (04/17/24)
    - Save Job - Related Jobs - Block Source