- Merck (Boston, MA)
- …scientists (including discovery research, biostatistics, drug metabolism, modeling and simulation, regulatory affairs , and global clinical trials operations) + ... Translational Medicine Operations, Translational Medicine-EU, Drug Metabolism/Modeling & Simulation, Regulatory Affairs , and late-stage Clinical Research throughout… more
- HNTB (Boston, MA)
- …protocols to ensure compliance with design criteria, scientific specifications, and regulatory approvals/permits. + Serves as senior reviewer of technical ... for local, state, and federal environmental permits as well as other regulatory compliance laws and regulations. + Organizes and participates in public meetings.… more
- Bristol Myers Squibb (Cambridge, MA)
- …the PC space + Manages relationships with key internal stakeholders including Regulatory , Clinical, Commercial, Medical Affairs & Communications and external ... after clinical proof-of-concept studies, including but not limited to regulatory submissions and life-cycle management. Translational disease strategies in… more
- ZOLL Medical Corporation (Chelmsford, MA)
- …and report/abstract/manuscript preparation and presentation + Mentor and supervise Research and Senior Scientists + Represent Scientific Affairs and ZOLL during ... time to be a part of ZOLL!Job SummaryThe Principal Scientist is responsible for planning, managing, analyzing, and presenting...a mentor to Research Scientists and will assist Scientific Affairs in the supervision of Research Scientists' work. The… more
- Merck (Boston, MA)
- …our Company, collaborating with project teams, biomarker leads, clinical operations, and regulatory affairs on the implementation of global CDx assay strategies ... **Job Description** In this Principal Scientist /Director position within Translational Oncology, this team member will provide leadership for aligned and integrated… more
- Novo Nordisk (Lexington, MA)
- …the Clinical Operations, Non-Clinical Research, Medical Writing, Program Management, CMC and Regulatory Affairs teams. Will be interfacing with both internal and ... with, Clinical Operations, Non-Clinical Research, Medical Writing, Program Management, CMC and Regulatory Affairs teams to deliver and drive the timely… more
- Amgen (Cambridge, MA)
- …closely with cross-functional teams, including R&D, manufacturing, quality assurance, and regulatory affairs , to ensure alignment and successful design transfer. ... Join us and transform the lives of patients while transforming your career. Senior Engineer, Design Transfer Specialist **What you will do** Let's do this. Let's… more
- Amgen (Cambridge, MA)
- …closely with cross-functional teams, including R&D, manufacturing, quality assurance, and regulatory affairs , to ensure alignment and successful design transfer. ... team. Join us and transform the lives of patients while transforming your career. Senior Engineer, Injection Molding Expert **What you will do** Let's do this. Let's… more