- Sanofi Group (Morristown, NJ)
- …and IVD products, intended to be used alone or in combination with a drug product, leading regulatory efforts in the development and post-marketing stages. The ... **Job title** : Global Regulatory Affairs Device Lead (Associate Director) **Location** :...of medicine? The race is on to speed up drug discovery and development to find answers for patients… more
- United Airlines (Arlington Heights, IL)
- …uninterrupted execution of Drug Abatement functions. As part of the Drug Abatement Regulatory & Compliance team, it emphasizes maintaining administrative ... overview and responsibilities** The role of Program Manager - Drug Abatement Administration, plays a critical role in ensuring...precision and operational efficiency to uphold regulatory compliance across all testing programs. + **… more
- University of Colorado (Aurora, CO)
- …**Condition of Employment:** **Preferred Qualifications:** + Experience with investigational drug services, clinical research operations, or IRB/ regulatory ... of pharmacy practice** with a particular interest in clinical research, investigational drug management, and regulatory compliance in academic or healthcare… more
- Lilly (Indianapolis, IN)
- …scientific degree (ie, PhD, PharmD) and 8+ years Industry-related experience in regulatory affairs and/or drug development experience OR + Bachelor's with ... 10+ years of industry-related experience in regulatory affairs and/or drug development experience **Other Information/Additional Preferences:** + Proven… more
- Bristol Myers Squibb (Cambridge, MA)
- …while ensuring early integration of precision medicine approaches-including coordination of key regulatory and clinical documents to support drug and diagnostic ... paired with deep expertise in developing and executing global regulatory strategies across drug and device development. + Regulatory Standards Mastery,… more
- University of Maryland, Baltimore (Baltimore, MD)
- …regulatory agency site visits. This program covers all major areas of drug product and biologics regulatory science, including: Chemistry, Manufacturing, and ... fulfill the faculty position of Instructor (non-tenure track) for the MS in Regulatory Science within the Department of Pharmaceutical Sciences. The MS in … more
- Takeda Pharmaceuticals (Boston, MA)
- …field. + Strong organizational, analytical, and communication skills. + Interest in regulatory strategy, drug development, and project management. + Proficiency ... my knowledge. **Job Description** RPM&SP partners with the Global Regulatory Lead (GRL) on Global Regulatory Teams...builds a strong foundation for a career in global drug development. **Job Requirements:** + This position will be… more
- Takeda Pharmaceuticals (Boston, MA)
- … 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)
- …related experience. + Experience in reviewing, authoring, or managing components of regulatory submissions. + Expert knowledge of drug development process and ... + Defines, develops and leads global strategies to maximize global regulatory success towards achievement of program objectives for complex and/or multiple… 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 a ... on patients worldwide. Join Takeda as a Director, Global Regulatory Lead Oncology where you will be part of...Oncology where you will be part of the global regulatory team. As Director, Global Regulatory Lead… more