Associate Director, RBQM Data Enablement and Analytics 3316 Takeda Development Center AmericasAssociate Director, RBQM Data Enablement and AnalyticsMassachusettsOversee strategic vendor and partner ecosystem in partnership with GDO Business Operations, including FSPs, CROs, and technology providers, setting performance expectations, governing delivery, and ensuring alignment to RBQM operating principles and outcomes. The actual base salary offered may depend on a variety of factors, including the qualifications of the individual applicant for the position, years of relevant experience, specific and unique skills, level of education attained, certifications or other professional licenses held, and the location in which the applicant lives and/or from which they will be performing the job.
Associate Director, Global Regulatory Affairs CMC 3316 Takeda Development Center AmericasAssociate Director, Global Regulatory Affairs CMCBoston, Massachusetts$154,400–$242,550 / yearProactively communicates CMC regulatory strategies, key issues and risks through assigned programs / products development activities and LCM in adequate and timely manner to cross-functional programs/ products teams and management level within GRA CMC, GRA, PS, GMS and QA - as appropriate. This role is within the Global Regulatory Affairs (GRA) Chemistry Manufacturing & Controls (CMC) and Devices organization, and will contribute to the team’s delivery of critical functions as follows: With minimal supervision, develops and leads the execution of regulatory CMC investigational, registration and/or post-approval strategies for assigned products.
Associate Director, Global Knowledge Management CSL Behring LLCAssociate Director, Global Knowledge ManagementWaltham, MAWe use three strategic scientific platforms of plasma fractionation, recombinant protein technology, and cell and gene therapy to support continued innovation and continually refine ways in which products can address unmet medical needs and help patients lead full lives. Focused on serving patients' needs by using the latest technologies, we discover, develop and deliver innovative therapies for people living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas.
Associate Scientific Director, DNA-Encoded Libraries 3316 Takeda Development Center AmericasAssociate Scientific Director, DNA-Encoded LibrariesBoston, MassachusettsThe role requires strong expertise in DEL selection, data analysis, hit identification, and collaborative drug discovery, as well as the ability to work effectively across medicinal chemistry, biology, biophysics, structural biology, computational chemistry, and related functions. This individual will design and execute DEL screening strategies, interpret DEL data, identify and prioritize chemical hits, and lead cross-functional efforts to advance validated hits through hit-to-lead.
Associate Director, Medical Training (Pipeline) Xenon PharmaceuticalsAssociate Director, Medical Training (Pipeline)Needham, MassachusettsOur Total Rewards program includes base salary, target bonus, and stock options, as well as a full range of benefits including medical, dental, vision, short-& long-term disability, accidental death & dismemberment, and life insurance programs, Employee Assistance Program, travel insurance, and retirement savings programs with company matching contributions. Training Module Development: Design and develop engaging training modules for different audiences and use-cases (field medical, sales, congress teams, cross-functional partners), incorporating adult learning principles, knowledge checks, and practical application exercises.
Associate Director, Commercial Learning - Psychiatry Alkermes PlcAssociate Director, Commercial Learning - PsychiatryWaltham, MAThe Alkermes Commercial Learning and Leadership Development (CL&LD) team is looking for someone who will lead the development of field training programs supporting Alkermes' growing portfolio of mental health treatments. Lead the identification, selection and day-to-day management of vendors as well as existing relationships and projects relating to field training (SOW and PO generation and vendor management).
Associate Director, Analytical Development & Quality Control Entrada TherapeuticsAssociate Director, Analytical Development & Quality ControlBoston, MassachusettsRemote$172,000–$202,000 / yearWe are a tight-knit team of experts and leaders in both therapeutic development and rare diseases and are excited to grow and attract colleagues who are ready to join a high-energy, dedicated team that likes to get things done and dramatically improve the lives of patients and their families. We expect multiple clinical data readouts as we advance several DMD programs across the U.K., EU, and U.S. By year-end 2026, we anticipate four clinical-stage programs in our DMD franchise (ENTR-601-44, ENTR-601-45, ENTR-601-50, and ENTR-601-51).
Sr. Manager/ Associate Director - Pharma SME Tiger Analytics LLCSr. Manager/ Associate Director - Pharma SMEBoston, MAThis role will serve as the functional expert across commercial data, Snowflake/lakehouse assets, reporting, and analytics while partnering closely with business and technology teams. Guide offshore teams and help establish governance, documentation, and delivery processes for the future analytics pod.
Sr. Manager/ Associate Director - Pharma SME Tiger AnalyticsSr. Manager/ Associate Director - Pharma SMEBoston, MAThis role will serve as the functional expert across commercial data, Snowflake/lakehouse assets, reporting, and analytics while partnering closely with business and technology teams. Guide offshore teams and help establish governance, documentation, and delivery processes for the future analytics pod.
Sr. Manager/ Associate Director - Pharma SME Tiger Analytics Inc.Sr. Manager/ Associate Director - Pharma SMEBoston, MAStrong experience with sales performance, patient services, speciality pharmacy, Veeva CRM, HCP/HCO, territory alignment, claims/prescription data , or related commercial domains. This role will serve as the functional expert across commercial data, Snowflake/lakehouse assets, reporting, and analytics while partnering closely with business and technology teams.
Associate Director, Quality Risk Specialist Bristol-Myers Squibb CoAssociate Director, Quality Risk SpecialistDevens, MA$175,310–$212,438 / yearThe Associate Director, RBQM - Hematology, Oncology, Cell Therapy, Immunology, Cardiology and Neuroscience will mainly be responsible for developing the Quality Narrative at the study and/or ASSET and Therapeutic Area levels to document end-to-end RBQM for critical to quality (CtQ) data, processes, and vendors, demonstrating effective risk and issue management. Project Management: Must be able to manage complex assignments/projects and effectively deliver all expected deliverables in a timely manner and proactively communicate changes in pre-established goals and deadlines.
After-School Assistant Site Director - Kid Care Andover Public SchoolsAfter-School Assistant Site Director - Kid CareAndover, MA$24–$27 / hourCandidates must be at least 20 years old and meet at least one of the following education and experience requirements: Hold a bachelor's degree in Child Development, Early Childhood Education, Elementary Education, Child Guidance, Human Services, Nursing, Psychology, Physical Education, Recreation, Child Psychology, the Arts, Social Work, Sociology, or Child Care and have at least six months of experience working with school-age children; Hold a bachelor's degree in any field or an associate degree in one of the fields listed above and have at least nine months of experience working with school-age children; or. Assistant Site Directors work closely with the Site Director to support daily program operations, guide staff, coordinate activities, maintain licensing and safety requirements, and build positive relationships with children, families, and school personnel.
Assistant Athletics Director, Fitness Center and Sports Performance Emerson CollegeAssistant Athletics Director, Fitness Center and Sports PerformanceBoston, MassachusettsAll Student Affairs staff are expected to actively participate in and support major divisional and institutional programs and events, including but not limited to student and staff training, Move-in and Move-out, Orientation, Family & Friends Weekend, Picture Yourself at Emerson, Commencement, the Student Organizations Fair, and other key community-building initiatives. The Assistant Athletics Director, Fitness Center & Sports Performance position reports to the Associate Athletics Director, Fitness Center & Sports Performance and will assist with maximizing student-athletes' athletic performance while reducing the risk of injury.
Associate Director, Payroll And Equity Amylyx PharmaceuticalsAssociate Director, Payroll And EquityCambridge, MARemote$163,000–$183,000 / yearReview and maintain the documentation of payroll reports, including semi-monthly, monthly, quarterly and year-end payroll reports (gross payroll, hours worked, accruals, tax deductions, benefit deductions, etc.). Payroll: Own the day-to-day processing of U.S. multi-state payroll using ADP, including garnishments, benefits and taxes to multi-site employees consistent with federal and state wage and hour laws.
Associate Creative Director Material BankAssociate Creative DirectorBoston, MAFlexible Work Schedules : With business units and employees across the globe, Material Technologies has embraced a hybrid working model allowing department leaders to decide on the best approach for their respective teams, whether that be remote, in person, or a little of both. As we launch a new platform, bring our refreshed brand identity to life, and expand to new audiences, you'll bring a strong creative point of view and help shape how Material Bank shows up in its next phase of growth.
NewAssociate Regulatory Affairs Director - Cell Therapy AstraZeneca PlcAssociate Regulatory Affairs Director - Cell TherapyCambridge, MA$135,624.80–$203,437.20 / yearAs a key member of the global regulatory strategy team (GRST), you are responsible for partnering with senior regulatory experts to support the end-to-end regulatory strategy planning, coordination, and execution of assigned cell therapy projects. The ARAD provides regulatory expertise and guidance on the clinical development requirements, including procedural and documentation requirements to regulatory and cross-functional teams, working flexibly within and across regions to achieve business objectives.
Lead, Market Access Analytics, US Oncology (Associate Director) 3312 Takeda Pharmaceuticals AmericaLead, Market Access Analytics, US Oncology (Associate Director)Boston, Massachusetts$154,400–$242,550 / yearThe US Oncology Market Access Analytics Lead will leverage data across multiple sources to create analyses, synthesize results into actionable insights, and communicate the business impact to cross-functional stakeholders to shape US Oncology Business Unit (OBU) Market Access strategies and enable Market Access field teams. Main activities include analysis of data from above brand Hub/Patient Services Programs, Trade & Distribution Operations, State & Federal policies (PBM reform, MFN, etc), and other emerging US healthcare landscape trends that impact the Oncology therapeutic area.
Associate Scientific Director, Synthetic Molecule DS Project Lead 3316 Takeda Development Center AmericasAssociate Scientific Director, Synthetic Molecule DS Project LeadCambridge, MassachusettsDigital fluency and independent, responsible use of approved generative AI tools: Demonstrated ability to leverage digital tools to improve cross-functional execution, transparency, and decision readiness; uses approved generative AI tools to accelerate preparation of governance-ready materials independently and responsibly, ensuring human review, traceability, and protection of confidential information, and may coach peers on effective use within applicable policies. In Pharmaceutical Sciences, Synthetic Molecule Process Development (SMPD) we develop and leverage the scientific expertise of our diverse talent to ensure patient safety and access to medicines through the design, development, and understanding of robust, sustainable, low-cost manufacturing processes, while ensuring on-time delivery of high-quality synthetic molecule drug substance.
Associate Director, Medical Program Management GI2 3316 Takeda Development Center AmericasAssociate Director, Medical Program Management GI2MassachusettsObjective/Purpose: Provide strategic program leadership at the asset level for complex Medical priorities, ensuring that TA and asset strategies are translated into executable program plans that are well-governed, transparent, and deliverable with clear accountability and disciplined decision-making. Serve as a core PMO partner to Therapeutic Area and Medical leaders, shaping execution approaches, governance frameworks, and cross-functional alignment for key programs, launches, lifecycle initiatives, and transformation efforts within assigned scope.
Associate Director, Medical Program Management 3316 Takeda Development Center AmericasAssociate Director, Medical Program ManagementMassachusettsObjective/Purpose: Provide strategic program leadership at the asset level for complex Medical priorities, ensuring that TA and asset strategies are translated into executable program plans that are well-governed, transparent, and deliverable with clear accountability and disciplined decision-making. Serve as a core PMO partner to Therapeutic Area and Medical leaders, shaping execution approaches, governance frameworks, and cross-functional alignment for key programs, launches, lifecycle initiatives, and transformation efforts within assigned scope.