- Takeda Pharmaceuticals (Boston, MA)
- …Nuclear Medicine, Radiologic Technology, Ultrasound, or MRI) preferred. + Experience in drug development and/or design and implementation of imaging in clinical ... to shine? Join us as a Research Scientific Associate Director , Clinical Imaging in our Cambridge, MA office. At...technologies in a "fit for purpose" manner in the drug development process. + Must have excellent… more
- Takeda Pharmaceuticals (Boston, MA)
- …through assay execution, data capture, analysis, and reporting. + **Biochemical Assay Development & Profiling** + Partner with Drug Discovery scientists in ... Drug Discovery Units (DDUs) to drive the design, development , and validation of robust biochemical assays (eg, enzyme,...OR BS with 18+ years of relevant experience in pharmaceutical or biotech R&D, with a strong focus on… more
- Takeda Pharmaceuticals (Boston, MA)
- …regulatory submissions including for Late-Stage assets. + Solid working knowledge of drug development process and regulatory requirements. Knowledge of FDA, EU, ... oncology portfolio with potentially first-in-class and best-in-class therapies, including antibody- drug conjugates (ADCs), complex biologics and small molecules. Our… more
- Takeda Pharmaceuticals (Boston, MA)
- …inclusive of regulatory and/or related experience. + Solid working knowledge of drug development process and regulatory requirements. Knowledge of FDA is ... medicines and make a lasting impact on patients worldwide. Join Takeda as a Director , Global Regulatory Lead Oncology where you will be part of the global regulatory… more
- Sanofi Group (Cambridge, MA)
- …and scientific communication at Global and Key Market level, preferred. + Broad drug development experience with robust knowledge of regulatory, market access ... **Job Title:** Global Medical Affairs Director - Oncology **Location:** Cambridge, MA / Morristown,...to success is an outstanding partnership with Countries, Clinical Development and Commercial to maximize the value proposition. Externally,… more
- Takeda Pharmaceuticals (Boston, MA)
- …of labeling content and strategy of multiple products in various stages of drug development , assigned to self or direct reports, including at least ... + Understanding of scientific principles and regulatory/quality systems relevant to drug development . + Ability to independently create, revise and/or… more
- Sanofi Group (Cambridge, MA)
- …to support critical trial decision-making and advance treatment across all phases of drug development . EGDS will support your growth through people ... **Job Title:** Statistical Project Leader (Associate Director ) **Location:** Morristown, NJ Cambridge, MA __ **About...or related discipline with at least 5 years of pharmaceutical experience in clinical development , including experience… more
- Takeda Pharmaceuticals (Boston, MA)
- …authoring, or managing components of regulatory submissions. + Expert knowledge of drug development process and regulatory requirements. Knowledge of FDA, EU, ... strategic and tactical advice to teams to achieve timely and efficient development and maintenance of programs, while ensuring compliance with applicable regulatory… more
- Takeda Pharmaceuticals (Boston, MA)
- …inclusive of regulatory and/or related experience. + Solid working knowledge of drug development process and regulatory requirements. Knowledge of FDA, EU, ... medicines and make a lasting impact on patients worldwide. Join Takeda as Associate Director , Global Regulatory Lead Oncology where you will be part of the global… more
- GRAIL (Boston, MA)
- …United Kingdom. It is supported by leading global investors and pharmaceutical , technology, and healthcare companies. For more information, please visit grail.com ... . The role assists with regulatory strategy and the development of submissions in partnership with key internal and external stakeholders for GRAIL projects,… more