- Takeda Pharmaceuticals (Boston, MA)
- …with the ability to make tough talent decisions. + Deep expertise in ** Regulatory Affairs , Clinical Development, and R&D technology ecosystems** (eg, Veeva Vault ... executing the vision, strategy, and delivery of technology solutions that enable global R&D, Regulatory , or Global Development functions. This role owns a… more
- AbbVie (Barceloneta, PR)
- …to use their broad understanding of Product Development, Manufacturing, Quality and Regulatory Affairs to translate the business objectives into actionable ... LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The ME&C Associate Director is a global program management expert responsible for… more
- BD (Becton, Dickinson and Company) (San Diego, CA)
- …communication skills (up, down, and outward) **Preferred Qualifications:** + Experience in Regulatory Affairs preferred. + Experience in metrics, data analytics, ... **Job Description Summary** The Associate Director , Quality Systems & Architecture will be responsible...subject guidance for our Tijuana, Otay, Vienna, and other global sites conducting QMS activities. **Job Description** We are… more
- Gilead Sciences, Inc. (Santa Monica, CA)
- …Partner across Kite Medical Affairs , Clinical Development, Translational Medicine, Regulatory Affairs , and Product Teams to build integrated cross-functional ... (IEP) for Kite assets in collaboration with the entire Evidence Generation Function, Global Medical Affairs Strategy and Product Teams. + Provide leadership to… more
- HRPivot (Tucson, AZ)
- …of GLP animal studies, preclinical testing, and clinical studies. + Partner with Regulatory Affairs and Clinical teams to support FDA PMA submissions and ... with hands-on experience managing GLP animal studies, clinical testing, and regulatory submissions. This is a high-impact leadership role shaping next-generation… more
- AbbVie (North Chicago, IL)
- …collaboration with cross-functional teams and counterparts in quality systems, regulatory affairs , medical writing, clinical development, clinical operations, ... contribution to post market surveillance activities, input to compliant regulatory authority reporting, development and implementation of lifecycle safety risk… more
- Danaher Corporation (New York, NY)
- …collaborating with cross-functional teams including Product Management, Legal, IP, Finance, R&D, Regulatory Affairs , Clinical Affairs , Sales & Marketing, ... of people worldwide - and we're using our unmatched global scale and proven playbook to make it happen,...to execute with supporting organizations (sales, commercial marketing, medical affairs , R&D, manufacturing, regulatory , quality, etc.) on… more
- Edwards Lifesciences (NY)
- …Conduct technical, product briefings for cross functional teams such as complaints, Engineering, regulatory affairs , quality affairs and clinical affairs ... **Sr. Director , Global Professional Education, Training -...understanding of product labeling content approval processes and systems, regulatory guidelines and legal boundaries + Expert understanding of… more
- J&J Family of Companies (Titusville, NJ)
- …Finance and Procurement, Global Commercial Strategic Organization, Global Medical Affairs , Regulatory Affairs , Research & Development, Global ... Medical and Scientific Communications Teams, US commercial partners, Cross US Medical Affairs Therapeutic Areas, Global Clinical Development Organization,… more
- Takeda Pharmaceuticals (Boston, MA)
- …communicate safety issues with other functional areas such as Clinical Development, Regulatory Affairs , Quality Assurance, Medical Affairs , Marketing, ... knowledge. **Job Description** **Objective:** **Principal responsibilities include:** + Serves as Global Safety Lead (GSL) and the Company-wide patient safety expert… more