- Merck (Boston, MA)
- …closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development projects; and ... company and competitors' drugs and internal and external expert opinion on scientific questions relevant to his/her areas of responsibility. **The Senior Director is… more
- Merck (Boston, MA)
- …closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development projects; and ... and competitors' drugs, and of internal and external expert opinion on scientific questions relevant to his/her areas of responsibility. **The Senior Director is… more
- Bristol Myers Squibb (Cambridge, MA)
- …Leadership organization are strategic-thinking, problem-solving, and action oriented scientific leaders who bring drug development and commercialization insights ... analysis and/or interpretation of clinical data and translation into scientific communication strategy, including publications, and commercial strategy. +… more
- Pfizer (Cambridge, MA)
- …role in regulatory policy priorities by representing Pfizer in appropriate scientific or regulatory activities (eg, membership in advisory councils and/or trade ... line help them achieve their full potential. **QUALIFICATIONS / SKILLS** + Advanced Scientific Degree (MD, Ph.D., PharmD) with a minimum of 10 years' experience in… more
- Merck (Boston, MA)
- …field-based employees such as the Vaccine Key Customer Leader (VKCL), Vaccine Medical Affairs Leader (VMAL), Region Medical Director (RMD) as well as other members ... and health care environment knowledge through self-study of company-provided scientific , product and marketplace information, attendance at product workshops and… more
- Takeda Pharmaceuticals (Boston, MA)
- …task-forces and initiatives. **Minimum Requirements/Qualifications:** + Bachelor's Degree required, scientific discipline strongly preferred, advanced degree in a ... managing components of regulatory submissions. + Understand and interpret complex scientific issues across multiple projects as it relates to regulatory requirements… more
- J&J Family of Companies (Danvers, MA)
- …("Voice of Investigator") to Abiomed cross-functional partners such as R&D, medical affairs , marketing, sales, and education. JOB DUTIES + Provides field support for ... technical, research, and organizational leadership qualities. + Collaborate with Clinical Affairs , Medical Affairs , R&D, marketing, and commercial teams to… more
- Takeda Pharmaceuticals (Boston, MA)
- …within the CoE of Global Medical. + Provides innovative thinking and scientific expertise into peri- and post-approval research programs and real-world evidence ... of a strategy for all study types within Global Medical, ie Medical Affairs Sponsored Studies (MACs). Also, develops Areas of Interest (AOI) for Collaborative… more
- Takeda Pharmaceuticals (Boston, MA)
- …manner, develops and executes a labeling implementation plan to incorporate new scientific , safety and clinical data, as well as Health Authority responses / ... at the Labeling cross functional teams, including clinical, safety, medical affairs , and commercial, to ensure unparalleled communication effectiveness for labeling… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …strategy, leading cross-functional study teams, and ensuring the highest standards of scientific and medical integrity. The incumbent will be responsible for the ... through late-stage trials and regulatory submissions. + Provide medical and scientific leadership to cross-functional study teams and ensure high-quality clinical… more