- Takeda Pharmaceuticals (Boston, MA)
- …silos, improve accessibility, and enhance agility across R&D while enabling compliance with regulatory standards such as HIPAA and GxP. + Implement and oversee fit ... insights, enhance decision-making, and drive efficiency across research, clinical, and regulatory functions. + Elevate Technical Skillsets: Serve as a mentor and… more
- Takeda Pharmaceuticals (Lexington, MA)
- …of analytical controls and compliance + Global CMC program oversight of Pharmaceutical Sciences (PS) with management and oversight of all project-related analytical ... to Commercialization by collaborating with multiple functions within the Pharmaceutical Science organization to improve analytical, process and product knowledge.… 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 ... transactional IP support, with an emphasis on patent litigation in the pharmaceutical /biotech industry. As a partner and key business strategist, this individual… more
- Takeda Pharmaceuticals (Boston, MA)
- …degree in a scientific discipline plus commensurate long-term experience within pharmaceutical or biotech industry + 5+ years healthcare or related experience, ... development and execution of medical publications, within medical affairs in the pharmaceutical or biotech industry or within a medical communications agency, is… more
- Merck (Boston, MA)
- …stakeholders to ensure alignment with clinical development timelines and regulatory requirements. Most importantly, the role requires overseeing CDx development, ... ensuring timely delivery of CDx solutions for pharmaceutical registration and launch. This individual is expected to stay up to date regarding industry trends and… more
- Takeda Pharmaceuticals (Boston, MA)
- …and monitoring processes, and ensuring compliance with corporate and regulatory standards. By maintaining high-quality standards, this role supports Takeda's ... your transition.** **How will you contribute:** + Ensure compliance to Regulatory Intelligence Procedures by executing the regulatory intelligence process… more
- Takeda Pharmaceuticals (Boston, MA)
- …Therapies in our Cambridge office. At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led ... to clinical development, taking into consideration the medical, scientific, regulatory and commercial perspectives. They will lead a multi-disciplinary,… more
- AbbVie (Worcester, MA)
- …to lead site analytics web and data quality initiatives within our pharmaceutical operation reporting into Digital Systems organization. This role is central to ... accurate, secure and in full compliance with AbbVie's global program and regulatory standards including FDA, EMA and MHRA requirements. This role bridges the… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …drive a MIDD path within each At Takeda, we are transforming the pharmaceutical industry through our R&D-driven market leadership and being a values-led company. To ... approaches (eg, QSP, MBMA) to inform internal decisions and external regulatory interactions. + Represents Clinical Pharmacology in meetings with global or… more
- Baystate Health (Greenfield, MA)
- …The primary responsibilities of the clinical pharmacist include providing comprehensive pharmaceutical care to all patients within Baystate Franklin Medical Center. ... clinical pharmacist will maintain competency, training, and ongoing education of pharmaceutical knowledge, integrated technology, and practice model changes. It is… more