- Takeda Pharmaceuticals (Cambridge, MA)
- …through close collaboration with cross-functional teams (including Medical Affairs, Clinical Development , Regulatory Affairs, Commercial, GPD comms), to ensure ... contents and cadence across TA compounds and programs. + Includes development of integrated medical communications plans including scientific publication strategy… more
- Cambrex High Point (Waltham, MA)
- …process intensification technologies. Our company is catalyzing the transformation of research , development , and manufacturing across the pharmaceutical and fine ... development Education, Experience & Licensing Requirements Education: + PhD . in Organic Chemistry, Chemical Engineering, Pharmaceutical Sciences, or related… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …teams, including process chemistry, analytical development , drug product development , manufacturing, quality assurance, and regulatory affairs, to develop ... or business processes. + Responsible for authoring relevant sections of regulatory documents, validation plans, development reports, process flow diagrams… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …- T1) or early development (phase 1) assets either within Medical Affairs, Regulatory Affairs, or Clinical Development is preferred. + Minimum of 7+ years of ... which is comprised of a strong portfolio of individual development and marketed assets. As we continue to develop...and strong competency with the US healthcare system and regulatory landscape is required for this role. + Stay… more
- Takeda Pharmaceuticals (Boston, MA)
- …Acumen** **:** + Provides scientific leadership and innovation in pharmaceutical research and development . Builds teams across functions and geographies ... only in technical expertise but across Takeda competencies. + Independently leads development of strategy and plans for multiple, complex programs + Regularly leads… more
- IQVIA (Boston, MA)
- …scientific reports from external sources for inclusion as a resource for content development . + Reviews clinical regulatory documents and comms + Understands ... branding objectives. Primary responsibilities include the management of projects, development of high-quality scientific content, partnering with stakeholders to… more
- Dana-Farber Cancer Institute (Boston, MA)
- …cutting-edge solutions that drive real-world outcomes for cancer treatment and research . Located in Boston and the surrounding communities, Dana-Farber Cancer ... is a leader in life changing breakthroughs in cancer research and patient care. We are united in our...+ Plan, advise and execute on scalable practices for development , deployment, and long-term monitoring for advanced analytics solutions,… more
- Sanofi Group (Cambridge, MA)
- …in the pharmaceutical or biotech industry working in Medical Affairs and/or clinical research and development . + Experience in planning, executing, and reporting ... the Solid Tumor Oncology portfolio, including products at various stages of development . + **Medical Affairs Expertise** : Provide medical affairs expertise for… more
- Bristol Myers Squibb (Devens, MA)
- …operation and maintenance of world-class facilities that enable the discovery, development and delivery of innovative medicines that help patients prevail over ... group, the successful applicant will be primarily responsible for the development of a company-wide approach to perform GLP environmental fate/effects studies… more
- AbbVie (Cambridge, MA)
- …of at least one aspect of Drug Development (eg, pre-clinical research , clinical development , Regulatory Affairs, Chemistry Manufacturing and Controls ... field required (eg PhD , PharmD, MD). + 2+ years of drug development or Business Development work experience in the pharmaceutical or biotechnology industries… more