• Director, Global Clinical Development-Rheumatology…

    Otsuka America Pharmaceutical Inc. (Albany, NY)
    …including immunology, biostatistics, clinical pharmacology, formulation science, data management, and medical writing . + Complete understanding of the global ... designs and protocols. + Develops focused expertise to serve as an clinical/ medical scientific consultant to health economic, medical affairs, marketing,… more
    Otsuka America Pharmaceutical Inc. (04/17/25)
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  • Investigator Initiated Trial Specialist - Clinical…

    Stony Brook University (Stony Brook, NY)
    …PhD in a related field + Additional experience in clinical research, including medical writing + ACRP/SOCRA certification (or equivalent) + Experience with ... requirements:** + Successfully complete pre-employment physical examination and obtain medical clearance from Stony Brook Medicine's Employee Health Services *… more
    Stony Brook University (05/31/25)
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  • Associate Director, Biostatistics - Hematology

    Regeneron Pharmaceuticals (Tarrytown, NY)
    …Clinical Scientists, Regulatory Affairs, Preclinical scientists, Statistical Programming, Data Management, Medical Writing , and others to design and analyze ... clinical trials. + Lead contributions to the preparation of material to be used in regulatory interactions, including drafting analysis plan and reviewing TFLs to be used in regulatory meetings, slides for advisory committee meetings, etc. + Lead and… more
    Regeneron Pharmaceuticals (05/29/25)
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  • Manager, Biostatistics

    Regeneron Pharmaceuticals (Tarrytown, NY)
    …Clinical Scientists, Regulatory Affairs, Preclinical scientists, Statistical Programming, Data Management, Medical Writing , and others to design and analyze ... clinical trials. + Developing individual protocols and statistical analysis plans and determines appropriate statistical methodology for data analysis. + Collaborating with Statistical Programming on the programming of tables, figures and listings to support… more
    Regeneron Pharmaceuticals (05/22/25)
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  • Director, Biostatistics - Internal Medicine

    Regeneron Pharmaceuticals (Tarrytown, NY)
    …Clinical Scientists, Regulatory Affairs, Preclinical scientists, Statistical Programming, Data Management, Medical Writing , and others to design and analyze ... clinical trials, as well as ensure the clinical program is appropriately designed. + Guides staff in the preparation of material to be used in regulatory interactions, including drafting analysis plan and reviewing TFLs to be used in regulatory meetings,… more
    Regeneron Pharmaceuticals (05/09/25)
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  • Senior Manager, Global Regulatory Affairs

    Otsuka America Pharmaceutical Inc. (Albany, NY)
    …members of the global regulatory team (GRL, regional leads, CMC-RA, labeling, medical writing , regulatory operations, etc.) to develop global regulatory plans, ... accordance with states and local laws. **Company benefits** : Comprehensive medical , dental, vision, prescription drug coverage, company provided basic life,… more
    Otsuka America Pharmaceutical Inc. (04/23/25)
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  • Director of Writing Colleagues Program

    Hobart and William Smith Colleges (Geneva, NY)
    The Writing Colleagues Program at Hobart and William Smith Colleges is a course-embedded tutoring program that is among the oldest in the country (est. 1993). The ... program supports writing across the curriculum through the training and mentoring...national origin, ancestry, sex (including pregnancy, childbirth, or related medical conditions), gender, gender identity or expression, age, sexual… more
    Hobart and William Smith Colleges (04/15/25)
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  • Principal Clinical Pharmacologist - ImmunoOncology

    Regeneron Pharmaceuticals (Tarrytown, NY)
    …analysis plans + Draft, finalize, and/or review CP reports + Collaborate with the Medical Writing Team to incorporate PK/PD sections into clinical study reports ... + Provide CP support of regulatory documents, communications, and presentations (eg, IND, health authority queries, preparation of BLA summary sections, addressing review inquiries) with SGD supervision + Represent CP at pre-IND, Type C, preBLA, and other… more
    Regeneron Pharmaceuticals (05/30/25)
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  • Sr. Scientific Writing Specialist

    System One (Tarrytown, NY)
    Title: Sr. Scientific Writing Specialist Location: REMOTE Schedule: M-F Full Time Type: Contract Responsibilities: + Drafts and manages reviews of submission ... degree or MS/PhD/PharmD in a life science + 0-2 years of scientific writing experience + Computer proficiency (Word, Excel, Adobe, and related software) and fluency… more
    System One (05/03/25)
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  • Downstream Process Associate (Chemistry Data…

    Eurofins (Rensselaer, NY)
    …+ Chemistry background is preferred. + cGMP experience and experience with technical writing is desirable. + Authorization to work in the United States indefinitely ... $19.50-22.50/hr. What we offer: + Excellent full time benefits including comprehensive medical coverage, dental, and vision options + Life and disability insurance +… more
    Eurofins (05/22/25)
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