- Otsuka America Pharmaceutical Inc. (Baton Rouge, LA)
- …+ Ensure regulatory intelligence specialists have continued access to regulatory, clinical trial , and public domain information resources to identify ... The Associate Director of Regulatory Intelligence leads the collection...may impact pharmaceutical practices, procedures and controlled documents. + Lead weekly regulatory intelligence team meetings to include review… more
- Reckitt (Salt Lake City, UT)
- Formulation Associate City: Salt Lake City **We are Reckitt** Home to the world's best loved and trusted hygiene, health, and nutrition brands. Our purpose defines ... of highly skilled talents that include Scientists, Engineers, Medical, Clinical and Regulatory professionals - all working to create...role** Want a role with real-world impact? As an associate within VMS formulation at RB, you'll have the… more
- AbbVie (North Chicago, IL)
- …the breadth of drug development (eg product development & manufacturing, trial design, evidence package evaluation, clinical acceleration, commercial ... team will have a direct impact on the future success of AbbVie. As Associate Director, Innovation, you will partner with leaders across AbbVie to optimize the value… more
- AbbVie (Mettawa, IL)
- …research delivery. + Utilize HEOR expertise and payer/HTA insights to shape clinical trial measurement strategies and interface with global regulatory bodies ... LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description Purpose: The Associate Director works independently with guidance from a Director and is… more
- Takeda Pharmaceuticals (Boston, MA)
- …orchestration to solve R&D challenges (eg knowledge extraction, medical writing, drug design, clinical trial optimization, etc. ). + Define and document the ... company to inspire you and empower you to shine? Join us as the Associate Director, Software Architect - AI/ML based in Cambridge, MA. **_GOALS_** _:_ We are… more
- Lilly (Indianapolis, IN)
- …develop innovative solutions to optimize manufacturing processes and increase capacity for clinical trial medicines, while also reducing costs and environmental ... impact. **Position Description:** The Associate Director Operational Readiness is responsible for managing the delivery of operational readiness aspects of the… more
- Veterans Affairs, Veterans Health Administration (Santa Rosa, CA)
- Summary The Lead Radiologic Technologist at the Santa Rosa, CA Community-Based Outpatient Clinic (CBOC) is responsible for coordinating all modalities within the ... VA Health Care System. They work closely with technologists, other lead technologists, radiologists, clinicians, and clerical staff to ensure optimal quality… more
- Lilly (Indianapolis, IN)
- …develop innovative solutions to optimize manufacturing processes and increase capacity for clinical trial medicines, while also reducing costs and environmental ... impact. The Associate Director - Analytical Quality Assurance ensures that laboratory...and the project schedule remains on track. **Responsibilities** + Lead a team of people which includes coaching/feedback for… more
- Veterans Affairs, Veterans Health Administration (Bay Pines, FL)
- …of the Business Office at the Bay Pines VA Healthcare System (BPVAHCS). The Lead MRT Coder assists in the planning, development, implementation, and maintenance of a ... coding quality assurance program. Responsibilities The Lead Medical Records Technician (Coder) Outpatient duties include, but...will be required to serve a 1 or 2-year trial period during which we will evaluate your fitness… more
- Lilly (Indianapolis, IN)
- …develop innovative solutions to optimize manufacturing processes and increase capacity for clinical trial medicines, while also reducing costs and environmental ... regulatory requirements while enabling advanced analytics and AI/ML capabilities + Lead cross-functional data governance council with representatives from PR&D, M&Q,… more