- United Therapeutics (Sacramento, CA)
- …are as follows:** Who we are We are the first publicly-traded biotech or pharmaceutical company to take the form of a public benefit corporation. Our public benefit ... a brighter future for patients through the development of novel pharmaceutical therapies; and technologies that expand the availability of transplantable organs.… more
- Otsuka America Pharmaceutical Inc. (Sacramento, CA)
- …role will champion operational rigor, foster strategic integration, and drive high- quality insights to support decision-making across the organization. Serving as a ... PhD) or equivalent preferred + Minimum of 15 years' experience in the pharmaceutical or biotechnology setting within medical affairs strategy + Sr Director level… more
- Otsuka America Pharmaceutical Inc. (Sacramento, CA)
- …with SMEs to interpret the impact of regulatory changes to the pharmaceutical environment. **Job Description** + Oversee the capture, review, and dissemination of ... opportunities, new and updated regulations and guidance that may impact pharmaceutical practices, procedures and controlled documents. + Lead weekly regulatory… more
- ThermoFisher Scientific (Carlsbad, CA)
- …and emerging industry developments that directly influence our business in pharmaceutical product development. Applying your expertise, you will actively contribute ... of relevant global regulations, guidelines, and evolving regulatory trends relating to pharmaceutical product development in the area of cell and gene therapy. +… more
- Sumitomo Pharma (Sacramento, CA)
- Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations in the US (Sumitomo Pharma America, Inc.), focused on addressing patient ... regulatory issues and provides possible solutions and mitigation strategy + Ensures the quality and content of all submissions to Health Authorities + Contributes to… more
- Cedars-Sinai (Los Angeles, CA)
- …May implement and coordinate department-wide initiatives such as research quality management or clinical trial recruitment efforts. Ensures compliance with ... committees. + Implement and coordinate department-wide initiatives such as research quality management or clinical trial recruitment efforts. + Provides guidance… more
- University of Southern California (Los Angeles, CA)
- …in order to ensure that project deliverables meet schedule, cost, scope, quality , and safety and ensuring continuous improvement by engaging all employees. Job ... for product testing. + Lead technology transfer to cGMP manufacturing and quality control, ensuring efficient scaling and implementation. Develop and review SOPs,… more
- Otsuka America Pharmaceutical Inc. (Sacramento, CA)
- …and the Senior Director to ensure timely and compliant submission of high- quality abstracts, posters, and manuscripts in line with Good Publication Practices (GPP) ... + Manage external vendors and medical writing agencies to ensure timely and high- quality content delivery. + Provide leadership and mentorship to a team of medical… more
- Otsuka America Pharmaceutical Inc. (Sacramento, CA)
- …best practices, ensure efficient processes, and support the delivery of high- quality medical plans. This role ensures alignment between scientific strategy, clinical ... Planning process, overseeing the development, integration, and communication of high- quality Medical Plans across multiple therapeutic areas + Establish and… more
- Taiho Oncology (Pleasanton, CA)
- …Biostatistics, PV, PK, Biomarkers and Medical Writing etc.), to deliver high quality clinical trial results. + Use scientific expertise to support the creation ... of relevant high- quality clinical documents such as study protocols and clinical...as required. Education/Certification Requirements: + Masters level degree in pharmaceutical or related medical science is preferred. Bachelor's level… more