- Pfizer (Cambridge, MA)
- …strategy and plan for the assigned molecule(s)/indication(s) + Responsible for scientific leadership and execution of clinical studies and delivering on innovative ... partners, such as project leaders, research units, biostatistics, regulatory affairs , clinical pharmacology, human genetics, translational oncology, precision medicine,… more
- J&J Family of Companies (Cambridge, MA)
- …disease modeling, and translational discovery. + Partner with clinical development and medical affairs to integrate RWE into evidence generation, supporting ... Johnson & Johnson Innovative Medicine is recruiting for **Senior Director , R&D Data Science & Digital Health - Ophthalmology.** This… more
- Sanofi Group (Cambridge, MA)
- …with cross-functional teams, including Market Access Shared Services, Brand Strategy, Medical Affairs , Regulatory, Patient Support Services, distribution and ... **Job Title:** Country Market Access and Pricing Senior Director , Access Strategy Amlitelimab **Location:** Cambridge, MA or Morristown, NJ **About the Job** The Sr.… more
- Sanofi Group (Cambridge, MA)
- …Teams to identify training needs and develop targeted solutions + Collaborate with Medical Affairs , Marketing, and Sales Training to ensure consistent messaging ... **Job Title:** Associate Director , Market Access Excellence **Location:** Cambridge, MA or...than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe. Discover… more
- Takeda Pharmaceuticals (Lexington, MA)
- …the best of my knowledge. **Job Description** **About the Role:** The Associate Director of Device Clinical Development (DCD) in the Drug Product and Device ... + Develop Device Clinical Development Strategy for Combination Products and Medical Devices + Develop comprehensive risk management strategies for devices and… more
- 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, ... my knowledge. **Job Description** **About the role:** The Associate Director , Clinical & Quality Process Compliance is responsible for...**What you bring to Takeda:** + BSc in a scientific or allied health/ medical field (or equivalent… more
- 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, ... Quality program leadership team. **What you bring to Takeda:** + BSc in a scientific or allied health/ medical field (or equivalent degree). + Minimum of 7… more
- Otsuka America Pharmaceutical Inc. (Boston, MA)
- … affairs , quality assurance, and other departments to drive scientific excellence, resolve complex technical issues, and ensure compliance with applicable ... **Associate Director , Small Molecule Analytical Development** + Lead and...a minimum of 5 business days. **Company benefits:** Comprehensive medical , dental, vision, prescription drug coverage, company provided basic… 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
- 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:**...than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe. Discover… more