- Pfizer (Cambridge, MA)
- …of related disciplines, eg, Clinical Operations, Safety, Biostatistics, Regulatory , Study Management, Pre-Clinical, Pharmacology, Quality Assurance. ... (POC) studies in Oncology. You will work in close collaboration with the Global Development Lead (GDL)and members of the development team to establish, lead,… more
- Bristol Myers Squibb (Devens, MA)
- …**Summary:** Bristol Myers Squibb is seeking an experienced and strategic Associate Director to lead the MES (Manufacturing Execution Systems) and Enterprise IT ... that support cell therapy manufacturing operations. + Ensure compliance with relevant regulatory requirements (GMP, GxP, 21 CFR Part 11) and internal standards for… more
- Manulife (Boston, MA)
- …a key role in strengthening governance and risk management. As part of our global team, you'll collaborate across North America and Asia in diverse areas such as ... makes a difference and helps shape the future at Manulife. Senior Director 's key responsibilities include planning, organizing, and assigning audit staff to projects… more
- Evolent (Boston, MA)
- …that convey insights effectively. + Partner with internal stateside and global teams to deliver high- quality analyses. **Required Qualifications:** + ... of our specialty programs and administrative platform. **Role Overview** The Senior Director role on Client Analytics will lead the development and execution of… more
- Sanofi Group (Cambridge, MA)
- **Job Title:** Associate Director , Consumer Marketing - US Rare Hematology **Location:** Cambridge, MA **About the Job** This role will drive consumer digital ... the consumer marketing lead for rare hematology. Sanofi is an innovative global healthcare company, committed to transforming the lives of people with… more
- Takeda Pharmaceuticals (Boston, MA)
- …+ Overseeing implementation of related processes and technologies in compliance with quality standards (including ICH GCP, local regulations, and Takeda SOPs). **How ... and conducting process impact assessments in response to changes in regulatory requirements identified through Takeda's regulatory intelligence activities, and… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …the best of my knowledge. **Job Description** **About the role:** The Associate Director , Commercial Engagements & P2P Strategy, offers a unique opportunity to shape ... external partners in a rapidly evolving market You will report to the Director , Head of HCP Engagements **How you will contribute:** + Champion Medical Communication… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …functional leadership, as part of the overall Asset Strategy in the Discovery, Global Product Teams, and Medical sub-teams through all stages of discovery, clinical ... physician-scientists, clinical leads, clinical pharmacologists, BST, discovery research scientists, regulatory , non-clinical and other functions to build consensus for… more
- AbbVie (Cambridge, MA)
- …the regulatory requirements related to the clinical studies and global drug development and accountable for complying with those requirements. May be ... Participates in cross-functional teams to generate, deliver, and interpret high- quality clinical data supporting overall product scientific and business strategy.… more
- Takeda Pharmaceuticals (Boston, MA)
- …with regulatory agencies. + Must have experience in global regulatory submission requirements and processes. **Program Leadership Skills/Competencies:** ... such as chemical engineering, analytical/organic/physical chemistry, process engineering, pharmaceutics, quality assurance and/or regulatory affairs. Advanced understanding… more
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