- Takeda Pharmaceuticals (Boston, MA)
- …of experience in GCP Quality/Compliance. + Advanced knowledge of pharmaceutical development, medical affairs and GCP/GVP regulations including FDA, EU, MHRA, ... best of my knowledge. **Job Description** **About the role:** Associate Director , Clinical Program Quality Investigations is responsible for ensuring the compliance… more
- Takeda Pharmaceuticals (Boston, MA)
- …among functions represented at the Labeling cross functional teams including clinical, safety, medical affairs , and commercial, to ensure the highest level of ... to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director , Global Labeling Lead where you will be responsible for the development… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …+ Continually evaluate Market Access strategies for pipeline products by partnering with Medical Affairs , Value and Evidence and the Market Access team while ... The Director , Value & Access Strategy leads the strategy...a minimum of 5 business days. **Company benefits:** Comprehensive medical , dental, vision, prescription drug coverage, company provided basic… 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 drug ... with analytical team members, process chemistry, formulation development, regulatory affairs , quality assurance, and other departments to drive scientific… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- **Job Description** The Senior Director , Strategy & Analysis; Contract Operations works cross-functionally to develop and execute pricing strategies for pipeline and ... and price on in-market and pipeline products. Works closely with Government Affairs to model/assess policy scenarios and evaluate the financial impact to Otsuka… more
- Lilly (Boston, MA)
- …in Boston, Massachusetts. **The Position** The purpose of the Associate Director , Regulatory Strategy role is to support the development and implementation ... for submissions, and taking part in meetings. + Represent the regulatory affairs team on cross-functional project teams and provide guidance to and oversight… more
- Rhythm Pharmaceuticals (Boston, MA)
- …barriers, together. Job Summary We are seeking a highly motivated and experienced Director of Data Science to lead data-driven initiatives in support of our ... with key inter-disciplinary stakeholders (eg biostatistics, clinical development and regulatory affairs ) to drive the generation of actionable data insights to… more
- Sanofi Group (Cambridge, MA)
- …product launch activities and strategic planning + Serve as key liaison between medical affairs , marketing, and commercial teams **About You** + Bachelor's ... **Job Title:** Associate Director , Product Strategy - Fabry and Gaucher **Location:** Cambridge, MA **About the Job** Lead strategic marketing initiatives focusing… more
- Takeda Pharmaceuticals (Cambridge, MA)
- …company that will inspire you and empower you to shine? Join us as Director , Quantitative Clinical Pharmacology (QCP) Lead in our Cambridge, MA office. Our Data and ... Sciences, Outcomes, Digital Health, Pharmaceutical Sciences/Device, and Global Regulatory Affairs . + Advanced knowledge of regulatory guidance for industry… more
- Takeda Pharmaceuticals (Boston, MA)
- …**Location: Cambridge, MA** **About the role:** As a Process Scientist (Associate Director ) - Global Manufacturing Science GMSci Drug Product (DP), you will provide ... Sciences + Global Manufacturing Supply, Global Quality and Global Regulatory Affairs . + SME for Takeda drug product manufacturing organization and network.… more