- Takeda Pharmaceuticals (Boston, MA)
- …through assay execution, data capture, analysis, and reporting. + **Cellular Assay Development & Profiling** + Partner with Drug Discovery scientists in Takeda's ... Drug Discovery Units (DDUs) to drive the design, development , and validation of robust cellular assays (eg, High Content, reporter, CTG, GPCR) for primary,… more
- State of Massachusetts (Everett, MA)
- …from the Director of Special Education Policy and Planning, the Senior Associate Commissioner of Special Education, will co-lead coordinating with OSEP ... will review during a scheduled onsite monitoring visit in 2025. The Senior Associate Commissioner will support the Director of SEPP to coordinate our efforts… more
- State of Massachusetts (Boston, MA)
- …The Senior Research Associate will also work closely with the EEC Director of Research and Senior Director of Data Analytics to develop and ... (EEC) seeks a contracted employee to serve as the Senior Research Associate to strengthen the agency's...Associate will work under the direction of EEC's Director of Research and collaborate closely with the Massachusetts… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …with cross-functional teams across the organization to drive and align the development and maintenance of global labeling (eg CCDS, regional product labels, and ... Strategy Lead, supporting preparation, review, and update of content for the development and maintenance of Company Core Data Sheet (CCDS), local labeling and… more
- Humana (Boston, MA)
- …Cloud and other skills IT Associates needs to succeed. + Partners with Associate Director to develop, refine, and prioritize the skilling roadmap, aligning ... all learning activities (Learning Needs Analysis to Design and Development and Delivery) to support associate skilling....availability allows, the rest of IT. + Supports the Associate Director in all reporting (eg, and… more
- GRAIL (Boston, MA)
- …please visit grail.com . The role assists with regulatory strategy and the development of submissions in partnership with key internal and external stakeholders for ... Lab Operations, and other stakeholders to support regulatory strategy development , product validation, audits, promotional material review, on-market product… more
- Takeda Pharmaceuticals (Boston, MA)
- …Communicates program status and issues to ensure timely decision-making by senior management. + May participate in Business Development /in-licensing/alliances ... lead the Clinical Sub Team (CST) accountable for the development and execution of the CDP. + Provide program-level...operations input into clinical documents related to the drug development process and into preparation for key regulatory meetings… more
- Takeda Pharmaceuticals (Boston, MA)
- …other stakeholders. The R&D Data and Quantitative Sciences organization influences senior leadership and stakeholders to advance Takeda's R&D pipeline. Central to ... to enhance efficiency and precision throughout the drug discovery and development lifecycle. It leverages cutting-edge technology, machine learning, AI, and… more
- Takeda Pharmaceuticals (Boston, MA)
- …of study build with quality deliverables per specification. Participate in the development , maintenance and training rendered on activities around study build and ... EDC systems and confirm adherence to established standards. **Testing Strategy Development :** + Develop and enhance testing strategies for EDC system study/library… more
- Lilly (Boston, MA)
- …teams (eg, Clinical, Regulatory, Supply Chain) to support the strategic development and execution of clinical programs. + Partner with cross-functional team ... part in data review and reconciliation efforts. + Contribute to the development and review of key regulatory documents (eg, Protocol, Investigator Brochure, Clinical… more