- Sanofi Group (Cambridge, MA)
- …marketing brand teams, market research , market access, medical affairs, business development , regulatory , research & development , manufacturing, ... maximize value for Sanofi + Lead and direct market development / shaping strategy, pre-launch and launch plans for...of a Bachelor's Degree is required. MBA, MS or PhD in life science is preferred + **Extensive and… more
- Guidehouse (Boston, MA)
- …all levels, to deliver product planning, pricing, reimbursement, product commercialization, and regulatory and compliance solutions. Do you think you are up for the ... business implications of new technologies and emerging trends; conducting primary research interviews with clinicians, thought leaders, and executives in the… more
- Bristol Myers Squibb (Cambridge, MA)
- …standing experience in all phases of research and drug development , including global regulatory submissions (IND/CTA through NDA/BLA/MAA/JNDA/ NDA China) ... Director, Program Management Lead (individual contributor) is assigned to high priority development asset(s). They operate as a strategic partner to the Global… more
- ZOLL Medical Corporation (Chelmsford, MA)
- …with cross-functional team members in scientific and clinical affairs, product development , regulatory , quality, and manufacturing. Essential Functions: * ... or related field with emphasis in biomedical signal processing; PhD degree preferred * 5+ years of experience in...* 5+ years of experience in signal processing algorithm development ; experience may include graduate degree research … more
- Oracle (Boston, MA)
- …and LLM agents for the healthcare sector. + Oversee the design and development of advanced agentic AI solutions tailored for healthcare applications, such as patient ... optimization, including advanced prompt engineering, model fine-tuning, and the development of sophisticated Retrieval-Augmented Generation (RAG) systems. + Collaborate… more
- Bristol Myers Squibb (Cambridge, MA)
- …experience in nearly all phases of research and drug development , including global regulatory submissions (IND/CTA through NDA/BLA/MAA/JNDA/ NDA China) ... **Position Summary** The Director, Program Management, is assigned to early and/or late development stage asset(s). They operate as a strategic partner to the Global… more
- Takeda Pharmaceuticals (Lexington, MA)
- …an author and reviewer. + Provide high quality of written study proposals, research and development reports, and investigation reports. + Support Validation ... a minimum of 3 years of experience. + A PhD in Chemical Engineering or related disciplines with 0...to definition of design space preferred + Experience in development and implementation of process control strategy using QbD… more
- Sanofi Group (Waltham, MA)
- …global vaccine development activities along the entire Value Chain from research up to market access + Strategic thinking and leadership abilities in combination ... internal (across Sanofi therapeutic areas) or external innovation solutions for the development of an Adjuvant platform for infectious disease targets + Close… more
- Cytel (Boston, MA)
- …as an industry leader by advancing **statistical methodologies for clinical development ** , promoting innovation, and enhancing **brand recognition** throughout the ... a team of consultants and analysts to define optimal ** regulatory , clinical, and/or market access pathways** . + Develop...in **Mathematics, Biostatistics** , or related field + Preferred: ** PhD ** , **MBA** , or **MD** + **Experience:** 10-15… more
- Takeda Pharmaceuticals (Boston, MA)
- …budget planning for Patient Access programs + Maintain awareness of worldwide Regulatory guidance and support implementation of best practices related to Patient ... teams and committees as assigned **Education, Behavioral Competencies and Skills:** **Required:** + PhD , PharmD with ~5+years; MS with ~8+ years; BS with ~10+ years… more
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