- Abbott (Alameda, CA)
- …Lingo is seeking an impactful Global Head of Quality and Regulatory Affairs to lead our innovative biowearables initiative and drive the next phase ... Abbott is a global healthcare leader that helps people...of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 114,000… more
- Takeda Pharmaceuticals (Boston, MA)
- …to bring life-changing therapies to patients worldwide. The Associate Director Global Regulatory Affairs , Neuroscience is responsible for developing innovative ... established andbuilding appropriate regulatory strategy. + Participates in cross-functionalinitiativeswithin Global Regulatory Affairs and Takeda R&D. **How you… more
- Sanofi Group (Morristown, NJ)
- …labeling leadership to cross-functional teams (Regulatory Strategy, Clinical Development, Medical Affairs , Pharmacovigilance, Market Access ). + Contribute ... **Job Title:** Director, Global Regulatory Affairs - Global...was possible. Ready to get started? **Main Responsibilities** + Lead the development, maintenance, and alignment of global… more
- AbbVie (North Chicago, IL)
- …Key Stakeholders Clinical development experts Statistical programmers Data science experts Global Medical Affairs experts Regulatory experts Additional ... that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a...from the North Chicago, IL AbbVie headquarters. Responsibilities: + Lead the statistical support for one or more clinical… more
- Sanofi Group (Morristown, NJ)
- …Director collaborates closely with cross-functional teams, including Global Regulatory Affairs , Clinical Development, Safety, and Medical Affairs , to ... **Job Title:** Associate Director, Global Regulatory Affairs - Global...was possible. Ready to get started? **Main Responsibilities** + Lead the preparation, review, and maintenance of global… more
- AbbVie (North Chicago, IL)
- …assigned projects. Specific areas of work may include clinical trials, patient safety, and global medical affairs . The Senior Manager works independently in ... medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's… more
- AbbVie (Irvine, CA)
- …projects. Specific areas of work may include clinical trials, patient safety, and global medical affairs . The Associate Director works in partnership ... medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's… more
- AbbVie (North Chicago, IL)
- …assigned projects. Specific areas of work may include clinical trials, patient safety, and global medical affairs (GMA). The Associate Director works in ... that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a...projects through own efforts or those of a team. Lead /develop statistical strategy for project development and regulatory submission.… more
- AbbVie (North Chicago, IL)
- …organization. Specific areas of work may include clinical trials, patient safety, and global medical affairs . The Manager works independently in partnership ... that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a...pre-planned safety analyses and ad hoc requests. + (SSG) Collaborate/ lead within the Safety Statistics Group to implement strategic… more
- Takeda Pharmaceuticals (Boston, MA)
- …therapies to patients worldwide. The Associate Director, Global Regulatory Affairs Advertising and Promotion (GRA A&P) Review Lead is accountable ... + As our Associate Director, Global Regulatory Affairs Advertising and Promotion lead you will...Advisor and function as the "R" in the core Medical , Legal, and Regulatory review functions within the Commercial… more