- Takeda Pharmaceuticals (Boston, MA)
- …is possible in order to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director Global Regulatory Lead, GRAD Oncology. You ... **How you will contribute:** + Defines, develops, and leads global strategies to maximize global regulatory...in collaboration with their regional counterparts. + As the Associate Director , you will be responsible for… more
- Takeda Pharmaceuticals (Boston, MA)
- …company that will inspire you and empower you to shine? Join us as an Associate Director , Global Regulatory Project Management and Strategic Planning ... - GI2 TAU within our Global Regulatory Affairs organization, based remotely. + Partners with the Global Regulatory Lead (GRL) on Global Regulatory… more
- Bristol Myers Squibb (Cambridge, MA)
- …both at work and in their personal lives. Read more: careers.bms.com/working-with-us . ** Associate Director , Global Regulatory Strategy, Neuroscience** ... **Position Summary:** The selected candidate will have leadership responsibility for global regulatory strategy within a development team (DT). Serve as team… more
- AbbVie (Cambridge, MA)
- …for a product(s) within Neuroscience and supports the Manager (Senior Manager, Associate Director , Director ( Global Regulatory Lead (GRL)), in the ... + Skill Set: Proven skill at implementing successful US and Canada regulatory strategies, global regulatory experience is a plus. Experience working in a… more
- Rhythm Pharmaceuticals (Boston, MA)
- …learn, and our tenacity to overcome barriers, together. Opportunity Overview In the Associate Director , Regulatory Affairs role, you will be responsible ... commercialization and life cycle of Rhythm products. This role reports into the Director , Global Regulatory Affairs. Responsibilities and Duties + Act as the… more
- Takeda Pharmaceuticals (Boston, MA)
- …to the best of my knowledge. **Job Description** ** Associate Director , US Advertising & Promotion Regulatory Review** **Takeda Pharmaceutical** ... the role:** Join Takeda as an Associate Director , US Advertising & Promotion Regulatory Review...regulations for development of marketing materials, including representation on global regulatory and labeling teams. + Provide… more
- Bristol Myers Squibb (Cambridge, MA)
- …more: careers.bms.com/working-with-us . **Position Responsibilities** + Leadership responsibility for global regulatory strategy to support the development of ... (HA) queries. + Ensure global development plans will meet global regulatory requirements by soliciting and integrating regional regulatory strategy… more
- Chewy (Boston, MA)
- …standards of regulatory compliance, quality assurance, and ethical sourcing. The ** Associate Director , Global Compliance & Ethical Sourcing** will define ... with R&D, Supply Chain, Operations, Legal, Marketing, and Quality. The Associate Director will also drive compliance investigations, supplier accountability,… more
- Takeda Pharmaceuticals (Boston, MA)
- …**Job Description** **OBJECTIVE / PURPOSE** + Providesprogram leadership and develops CMC regulatory strategy in support of global vaccine programs in various ... product developmentprogramspreferred + Sound understanding of scientific principles and regulatory CMC requirements relevant to global vaccine development,… more
- Takeda Pharmaceuticals (Boston, MA)
- …what is possible in order to bring life-changing therapies to patients worldwide. As Associate Director , Global Labeling Devices, you will be responsible for ... regulatory requirements. Serve as the expert for device labeling on the global Regulatory Affairs (RA) Sub team and Global Device Sub team (GDT) to… more
- Takeda Pharmaceuticals (Boston, MA)
- …possible in order to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director , Global Labeling Lead where you will be ... escalates issues to Global Labeling management and the Global Regulatory Lead (GRL) and proposes risk mitigation strategies for assigned products… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- **Position Overview** Otsuka is seeking an exceptional Associate Director of Global Medical Affairs (GMA) Excellence & Operations to support our emerging ... Quality Assurance** + Ensure all GMA operations activities comply with global regulatory requirements and company policies + Develop and implement quality… more
- Takeda Pharmaceuticals (Boston, MA)
- …leadership at LOC level Decision-making and Autonomy + Responsibility in line with Associate Director level position; independently lead HE projects and support ... Access, Global Evidence and Outcomes, Medica Affairs, Clinical Development, Regulatory Affairs, Biostatistics, Global Emerging Markets (GEM; eg, China),… more
- Takeda Pharmaceuticals (Boston, MA)
- …company that will inspire you and empower you to shine? Join us as an Associate Director , Global Evidence and Outcomes in our Cambridge, MA office. ... people to realize their potential through life-changing work. Certified as a Global Top Employer, we offer stimulating careers, encourage innovation, and strive for… more
- Takeda Pharmaceuticals (Boston, MA)
- …is true to the best of my knowledge. **Job Description** **Objectives/Purpose** The Associate Director , Global Medical Communications, Immunology is a key ... for assigned assets. In strategic partnership with cross-functional stakeholders, the Associate Director , Global Medical Communications, Immunology will:… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …assigned compounds to drive alignment of labeling content and strategy. + Partner with Global Regulatory Affairs to ensure that all labeling is aligned with the ... activities related to all global labeling components. + Represent Global Labeling on product-specific Regulatory and Cross-Functional teams, as appropriate.… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …is true to the best of my knowledge. **Job Description** **OBJECTIVES:** Global Evidence and Outcomes (GEO) contributes to the successful development and ... plans, scientific reports, briefing packages, clinical study reports, and regulatory labelling interactions. + Provide expertise and guidance on observational… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …and academic translational clinical research experience (as a general guideline, 1-3 years for Associate Director level; 3-6 years for Director is typically ... While not essential, prior personnel management experience, will support position at entry ( Associate Director / Director ). + An advanced understanding of drug… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …and/o academic translational clinical research experience (as a general guideline, 1-3 years for Associate Director level; 3-6 years for Director and 6-9 ... While not essential, prior personnel management experience, will support position at entry ( Associate Director / Director ). + An advanced understanding of drug… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …matrix teams + Diplomacy and positive influencing abilities Knowledge + Regional/ global Regulatory requirements + GCP/ICH This position is ... and empower you to shine? Join us as an Associate Medical Director , Clinical Science in our...Director leads and drives strategy for the overall global clinical development of assigned Takeda pipeline compound(s) taking… more