Jason Wall

Associate Director, Scientific Writing at Bristol Myers Squibb

Based in Seattle, United States

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Seniority

Director

Department

Science

Location

Seattle

Industry

Pharmaceutical Manufacturing

Company size

38K

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Email

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j•••••••@bms.com

Phone

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Background

About Jason Wall

Experienced Translational Science Leader with over 15 years of experience studying tumor biology, the tumor microenvironment, and the immune system. Experienced in biomarker strategy development supported by assay development and validation, applied against oncology and inflammation pre-clinical and clinical goals. Advanced studies in pre-clinical settings through registrational trials, including interactions with the FDA, EMA, and PMDA across multiple modalities such as immune-oncology modulators, antibody drug therapeutics, small and large molecule inhibitors and engineered cell therapies. Key Skills Experienced in assay development and validation applied both internally and outsourced with CROs- Multiplexed methods for characterizing complex immune subsets in peripheral blood, bone marrow, and the tumor micro-environment in tissue biopsies- Assessment of soluble factors (e.g. cytokines, or soluble target) using plate-based assays. Deep understanding of intracellular and apoptotic signaling, molecular biology, and proteomic applications. Assay applications spanning execution in clinical studies through in vitro, ex vivo and in vivo models. Team leadership through direct and indirect reports as well as working though complex organizational matrices. Selected Achievements Developed and validated fit-for-purpose biomarker assays supporting pre-clinical and clinical endpoints. Provided analysis that guided clinical trial decisions, patent and IND filing, and registrational submissions. Implemented biomarker strategy and assay application across solid tumor and hematologic indications (Multiple myeloma, NHL [DLBCL, CLL, MCL, FL], ALL, bladder, lung, head and neck, sarcoma, and breast cancer) Authored CSRs, supplemental reports, CTD summary documents, and responses to Health Authority queries, supporting successful drug approvals with multiple regulatory agencies.

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