- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …**Qualifications** + Bachelor's degree + 5-7 years of experience in pharmaceutical or healthcare industries, with experience in payer and/or channel functions ... required + Performance tracking and quarterly business review development experience + Experience working in matrix management structure with project management,… more
- Sanofi Group (Cambridge, MA)
- …health through chasing the miracle of science. As a prominent pharmaceutical manufacturer, our commitment extends beyond drug development, ensuring that patients ... case escalations + Identify and provide analysis and performance review of programs. + Plan, develop and coordinate Quarterly...patient support services, or a related field within the pharmaceutical or healthcare industry. . 5 or more years… more
- Sumitomo Pharma (Boston, MA)
- Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the US (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma ... and technical expertise in the area of oncology through review of the scientific literature and attendance at key...+ 3+ years of relevant experience in biotech or pharmaceutical industry + 3+ years of MSL experience in… more
- Sanofi Group (Cambridge, MA)
- …scientific knowledge and shaping health authority perspective as applied to the pharmaceutical industry. We are an innovative global healthcare company with one ... safety pharmacology, and the regulatory environment. + Provide authorship and/or expert review of white papers or regulatory submission documents as needed. +… more
- Sanofi Group (Cambridge, MA)
- …clinical activities, eg protocol development, pressure test and cluster feasibility, medical review and validation of clinical data , study risk assessment + ... to clinical studies such as medical training, feasibility, medical review of data , medical information for the...in the field of autoimmune diseases + Understanding of pharmaceutical product development and life cycle management gained through… more
- Sanofi Group (Cambridge, MA)
- …teams accelerate progress. This individual will be responsible for providing regulatory review and approval of US promotional and other product and disease-related ... Affairs (US RA AdPromo) as a member of cross-functional brand and portfolio team review committees (RC), providing regulatory input into the review and approval… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …aspects of upstream process technology transfers to CDMOs, including documentation review , gap analysis, and risk assessment. + Provide expert technical oversight ... of upstream manufacturing operations at CDMOs, including review of batch records, deviation investigations, and change controls. + Lead or significantly contribute… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …aspects of downstream process technology transfers to CDMOs, including documentation review , gap analysis, and risk assessment. + Provide expert technical oversight ... of downstream manufacturing operations at CDMOs, including review of batch records, deviation investigations, and change controls. + Lead or significantly contribute… more
- Takeda Pharmaceuticals (Boston, MA)
- …Excellence in our Cambridge office. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led ... and optimization of teams within Research. The incumbent will drive continuous review and reporting of Research business activities and support operational needs of… more
- Lilly (Boston, MA)
- …establish starting doses, dose ranges and in interpreting emerging human PK/PD data to inform dose escalation and dose regimen selection for proof-of-concept ... studies. + Author, review and approve key documents, including protocols, risk profiles,...relevant medical and scientific literature; know the status and data from relevant competitive assets and keep updated with… more