- Boehringer Ingelheim (Ridgefield, CT)
- …field with eight to ten (8-10) years' experience in the pharmaceutical industry in Regulatory Affairs or scientific discipline required OR Master's degree with a ... Boehringer Ingelheim's high regard for our employees. The Associate Director , DRA Product Labeling will lead and...six (6) years' experience in the pharmaceutical industry in Regulatory Affairs or scientific discipline required. +… more
- Takeda Pharmaceuticals (Boston, MA)
- …in order to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director , Global Labeling Lead where you will be responsible for the ... of labeling documentation and assures that Takeda labeling content and processes conform to regulatory ...Labeling cross functional teams including clinical, safety, medical affairs , and commercial, to ensure the highest level of… more
- Otsuka America Pharmaceutical Inc. (Princeton, NJ)
- …for new products. Preferred **Knowledge and skills** + Solid understanding of pharmaceutical regulatory affairs , global labeling regulatory requirements ... Drive Labeling Strategy, in-line with overall global regulatory strategy, by providing labeling expertise for Company Core Data Sheet (CCDS), USPI and local … more
- Lundbeck (Deerfield, IL)
- Associate Director Medical Affairs - Neurology Requisition ID: 7013 Location: Deerfield, IL, US Do you want to join a team where the mission is meaningful, the ... to candidates anywhere in the greater United States** **SUMMARY:** The Associate Director , Medical Affairs , Neurology serves as the internal scientific expert… more
- Evident Scientific (Needham, MA)
- …supporting submissions, inspections, and QMS compliance activities. Reporting to the Global Director of Regulatory Affairs - Clinical Business, the ... Sr. Mgr., Regulatory Affairs (RA) & Clinical ...clinical evidence synthesis. + Ensure alignment between clinical data, labeling , and regulatory claims. **Post-Market Compliance &… more
- CSL Behring (King Of Prussia, PA)
- As the Senior Director , Medical Affairs , you will lead the development and execution of Medical Affairs strategies and tactics to support the assigned US ... + Review and approve medical and scientific content of Regulatory , Safety, Scientific Affairs , Medical Affairs...the assigned disease area. + Provide input on US labeling and regulatory strategy. + Maintain in-depth… more
- Chiesi (Cary, NC)
- …consisting of cross-functional medical colleagues including provides medical input on US labeling and regulatory interactions + Ensures timely and appropriate ... of this role is to lead the PAH/PH-ILD US Medical Affairs team, ensuring alignment with Global Medical Affairs to execute the medical operating plan and Medical … more
- Coty (Morris Plains, NJ)
- …part of the global ingredient policy development and defense. This position reports to the Director , NA Regulatory Affairs and R&D Material Management and is ... Senior Manager, US Regulatory Affairs and Ingredient Support **SENIOR...retailers. + Provide guidance to Product Development regarding OTC labeling and claims. Including working with the global artwork… more
- Lilly (Indianapolis, IN)
- …make life better for people around the world. **Purpose:** The purpose of the Senior Director Global Regulatory Affairs , Global Regulatory Lead (GRL) ... leadership behaviors and regulatory excellence attributes as described in Global Regulatory Affairs white papers. + Constructively challenge teams to reach… more
- Lilly (Indianapolis, IN)
- …make life better for people around the world. **Purpose:** The purpose of the Senior Director , Global Regulatory Affairs , Global Regulatory Lead (GRL) ... leadership behaviors and regulatory excellence attributes as described in Global Regulatory Affairs white papers. + Participate in forums that share … more