- Takeda Pharmaceuticals (Boston, MA)
- …company to inspire you and empower you to shine? Join us as the Associate Director , Software Architect - AI/ML based in Cambridge, MA. **_GOALS_** _:_ ... compliant software platforms that drive discoveries, optimize decision-making, and streamline clinical and real-world evidence analysis. At the ShinrAI Center, we're… more
- Bristol Myers Squibb (Cambridge, MA)
- …more: careers.bms.com/working-with-us . **Key Responsibilities:** In the role as Associate Director , Companion Diagnostics Program Management within Precision ... team and deliverables, working effectively with cross-functional representatives including scientific , clinical , regulatory, legal, finance + Responsible for… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- ** Associate Director , Small Molecule Analytical Development** + Lead and oversee phase appropriate method development and optimization for drug substance and ... regulatory affairs, quality assurance, and other departments to drive scientific excellence, resolve complex technical issues, and ensure compliance with… more
- Bristol Myers Squibb (Devens, MA)
- …and in their personal lives. Read more: careers.bms.com/working-with-us . The ** Associate Director , Product Technical Steward, Cell Therapy Technical Operations ... control and implementation, product comparability and escalated support of technical/ scientific process and analytical issues + Regulatory & Documentation: Provide… more
- Takeda Pharmaceuticals (Boston, MA)
- …(from statistics, programming, outcomes research and epidemiology, quantitative clinical pharmacology, digital strategy, library sciences and data ... with our quantitative skills. We design efficient trials, contribute to clinical development strategies, perform high quality statistical analyses, and pursue… more
- Takeda Pharmaceuticals (Boston, MA)
- …improvement + Lead CPMQ continuous improvement initiatives to enable optimization of clinical and safety quality compliance activities. + Provide expert advice and ... metrics for CPMQ activities eg audit, inspection, QE, CAPA. + Organise Clinical and Pharmacovigilance Quality council meetings and proactively manage the agenda and… more
- Sumitomo Pharma (Boston, MA)
- …or follow us on LinkedIn. **Job Duties and Responsibilities** + Lead on clinical studies and manage/provide training to team members when needed. + Contribute and ... SAS/SQL and SAS/ODS. + Interact with Statisticians and other clinical teams, perform ad hoc analysis and generate +...plus. + BS/MS or equivalent in Statistics, Math or Scientific Discipline The base salary range for this role… more
- Bristol Myers Squibb (Devens, MA)
- …to support process data trending programs for the commercial and late stage clinical products across the cell therapy network. This individual will be responsible ... writing and technical presentations, contributing to broader external and internal scientific community as appropriate. Experience in generating formal reports and… more
- Grifols Shared Services North America, Inc (Fall River, MA)
- … Director , or equivalent) and proven history of success required. + Strong science/ clinical background with advanced degree in a scientific field of study ... and regions. The primary responsibility of the MSL Field Director is the management, performance, and coaching of a...but are not limited to:_ + Ultimate responsibility for scientific knowledge of self/team and oversight of a team… more
- Lilly (Boston, MA)
- …validation, enabling the diagnosis and treatment of neurodegenerative conditions. As Executive Director (or potentially Associate Vice President) you will drive ... influence both internal and external stakeholders. + Demonstrated ability to translate scientific insights into impactful clinical applications. Join Lilly in… more
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