- Sanofi Group (Cambridge, MA)
- …within the Sanofi portfolio of products. The team is part of the Global Regulatory Affairs , Regulatory CMC and Device Department within Global Research ... a highly professional global environment. **Skills/Qualifications** + MS degree -in a scientific or engineering discipline -with 6 years regulatory experience,… more
- Merck (Boston, MA)
- …Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... including development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Senior Director… more
- Sanofi Group (Cambridge, MA)
- …team and internal partners such as clinical operations, translational medicine, regulatory affairs , biostatistics, drug discovery, drug safety, marketing. + ... **Job Title:** Clinical Research Director **Location** : Morristown, NJ Cambridge, MA **About...with clinical operations. The CRD is expected to advance scientific and clinical knowledge for immunology in Dermatology, incorporate… more
- Sanofi Group (Cambridge, MA)
- …team and internal partners such as clinical operations, translational medicine, regulatory affairs , biostatistics, drug discovery, drug safety, marketing + ... **Job Title:** Clinical Research Director , I and I, IBD **Location:** Cambridge, MA...with clinical operations. The CRD is expected to advance scientific and clinical knowledge for immunology, and to incorporate… more
- Takeda Pharmaceuticals (Boston, MA)
- …Drug Safety, Clinical Sciences, Outcomes, Digital Health, Pharmaceutical Sciences/Device, and Global Regulatory Affairs . + Advanced knowledge of regulatory ... that will inspire you and empower you to shine? Join us as Associate Director , Quantitative Clinical Pharmacology (QCP) Lead in our Cambridge, MA office. At Takeda,… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …as a clinical/medical scientific consultant to health economic, medical affairs , marketing, regulatory , statistical and other research project team members, ... the following: + Consult with patients or their representatives, clinical, regulatory , and scientific leaders and thoughtfully apply their recommendations… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- …as an clinical/medical scientific consultant to health economic, medical affairs , marketing, regulatory , statistical and other research project team members, ... **Job Description** Otsuka is seeking a Director , Global Clinical Development (GCD), who will be...following: + Consults with patients or their representatives, clinical, regulatory , and scientific leaders and thoughtfully applies… more
- Takeda Pharmaceuticals (Lexington, MA)
- …program management experienced in leading cross-functional clinical programs within Medical Affairs , Clinical Research, Regulatory , CMC or other drug development ... phases of development with significant experience within related functions (eg, Medical Affairs , Clinical Operations, Regulatory , CMC, Marketing). + Minimum of 5… more
- AbbVie (Cambridge, MA)
- …as Discovery, Preclinical Development, Clinical Development, Process Development, CMC, or Regulatory Affairs . Must possess solid foundation of generally accepted ... development or marketed. S&E is responsible for conducting all scientific /technical due diligence to ensure an in-depth understanding of...a major revenue driver for the company. The Senior Director , Search & Evaluation will lead the Oncology S&E… more
- Bristol Myers Squibb (Cambridge, MA)
- …(Masters, PhD, PharmD, BSN, etc.) with at least 3+ years of Regulatory Affairs experience in the pharmaceutical industry. **Key Competency Requirements** ... in their personal lives. Read more: careers.bms.com/working-with-us . **Associate Director , Global Regulatory Strategy, Neuroscience** **Position Summary:** The… more