- BioSpace (Boston, MA)
- …provider's needs, enhance patient experience, and remain compliant with company and regulatory standards. As the Associate Director , Patient Services ... grounded in purpose and be empowered to deliver your best. Join Takeda as the Associate Director , Patient Services Operations out of our Cambridge, MA office. As… more
- Takeda Pharmaceutical Company Limited (Lexington, MA)
- …employment application is true to the best of my knowledge. Job Description Associate Director , Clinical Research, Value & Evidence Generation, US Medical ... applicable internal legal and compliance policies as well as external US-specific regulatory guidelines. Partners with US Medical TA leadership to determine project… more
- Alkermes (Waltham, MA)
- Job Description JOB DESCRIPTION Position Summary As an Associate Director within the INDIGO | AI Innovation Lab, you will lead the development and scaling of ... Preferred Qualifications Experience in pharmaceutical / biotechnology industry Familiarity with regulatory and compliance standards for data use in healthcare or… more
- Takeda Pharmaceutical Company Limited (Lexington, MA)
- …to bring Better Health and a Brighter Future to people worldwide. As an Associate Director in Analytical Development, you will lead efforts to develop advanced ... by Design (AQbD) principles, aligning with ICH Q14, ICH Q2(R2), and global regulatory expectations for biologics. Lead technical assessments and risk analyses to… more
- Nature Careers (Cambridge, MA)
- …the statistical support required by the development strategy under the supervision of the Associate Director or Director . They also contributes to the ... the preparation of responses to statistical issues arising in regulatory or other legal settings, or from external development...Employee Resource Groups participation Why Biogen? We are a global team with a commitment to excellence, and a… more
- Mythic Therapeutics (Waltham, MA)
- Associate Director , Clinical Operations Company Overview: Mythic Therapeutics is a privately held, clinical stage product-platform company building a pipeline of ... Job Summary: Mythic Therapeutics is searching for a dynamic Associate Director (AD), Clinical Operations to join...and detailed plans and ensuring the robust execution of Global clinical studies in accordance with timeline, budget and… more
- Sanofi Group (Cambridge, MA)
- **Job Title:** Associate Director , Global Regulatory Affairs - Global Labeling Strategy **Location** : Morristown, NJ or Cambridge, MA (Hybrid) ... families. Your skills could be critical in helping our teams accelerate progress. The Associate Director , Global Regulatory Affairs - Global Labeling… more
- Takeda Pharmaceuticals (Boston, MA)
- …what is possible in order to bring life-changing therapies to patients worldwide. The Associate Director Global Regulatory Affairs, Neuroscience is ... responsible for developing innovative global regulatory strategies and providing strategic regulatory guidance...and Takeda R&D. **How you will contribute:** + The Associate Director will be responsible for increasingly… more
- Takeda Pharmaceuticals (Boston, MA)
- …what is possible in order to bring life-changing therapies to patients worldwide. The Associate Director , Global Regulatory Affairs Advertising and ... to prescription medicine promotion. **How you will contribute:** + As our Associate Director , Global Regulatory Affairs Advertising and Promotion lead… more
- Sanofi Group (Cambridge, MA)
- **Job Title:** Associate Director , Global Regulatory Affairs Advertising and Promotion **Location** : Cambridge, MA Morristown, NJ **About the Job** Are ... was possible. Ready to get started? **Main Responsibilities:** + Represents Global Regulatory Affairs (US RA AdPromo) as a member of cross-functional brand… more
- Takeda Pharmaceuticals (Boston, MA)
- …my knowledge. **Job Description** **Objective / Purpose:** + Defines, develops and leads global strategies to maximize global regulatory success towards ... + Provides leadership and development for direct reports, including those that serve as global regulatory leads responsible for the design and execution of … more
- Takeda Pharmaceuticals (Boston, MA)
- … Global Regulatory Affairs CMC team, you will report to the Senior Director Global Regulatory Affairs CMC. **How you will contribute:** + Plan, ... in order to bring life-changing therapies to patients worldwide. Join Takeda as an Associate Director , GRA CMC Small Molecules where you will oversee the… 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
- Regeneron Pharmaceuticals (Cambridge, MA)
- Regeneron Cell Medicine is looking for an Associate Director in Regulatory CMC for biologics who will be responsible for the development and submission of ... to regulatory health authorities. + Leads the development of global CMC regulatory science-based strategies for internal RCM oncology investigational… more
- Takeda Pharmaceuticals (Boston, MA)
- …the development of scientific communications strategy and deliverables, the ** Associate Director , Scientific Communications Lead, Hematology** proactively ... empowered to deliver your best. As part of the Global Medical Affairs Oncology team, you will report to...in life sciences, and excellent project management skills. The Associate Director , Scientific Communications Lead, develops and… 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)
- …is true to the best of my knowledge. **Job Description** **OBJECTIVES:** Global Evidence and Outcomes (GEO) contributes to the successful development and ... analysis plans, scientific reports, briefing packages, clinical study reports, and regulatory labelling interactions. + Provide technical expertise and guidance on… 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 (Boston, MA)
- …+ Managesanyreportingstaff(Takeda employeesand/orcontractors). + Preparesorsupervisespreparationofhigh-quality DP-CMCsectionsfor Global regulatory filings to ... knowledge. **Job Description** **Objective:** Under the direction of the Director or Sr. Director , ODPD, the Assoc....knowledge of current GMP regulations. + Detailed knowledge of Global regulatory requirements for drug products. +… more
- Merck (Boston, MA)
- …component of decision-making at our Company, this position offers an opportunity for the Associate Director to drive pipeline impact across therapy areas. This ... Associate Director will work with scientists within...analyses + Developing and maintaining a comprehensive understanding of global regulatory expectations for small molecules and… more
