- CSL Behring (King Of Prussia, PA)
- …developing therapies that make a meaningful difference worldwide. Could you be our next Associate Director , PV Standards and Governance? The job is in our King ... (PV) data and processes. You will ensure compliance, consistency, and quality in safety data management across the R&D organization, supporting regulatory… more
- IQVIA (New Providence, NJ)
- …and patient outcomes. Learn more at https://www.iqviadigital.com. Join us as an ** Associate Director , Solutions Engineering** , where you'll lead a ... and reporting landscape. \#IQVIADIGITAL IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life… more
- Otsuka America Pharmaceutical Inc. (Princeton, NJ)
- **The R&D Strategic Sourcing Associate Director ,** Supplier Relationship Management is a pivotal role responsible for ensuring compliance with procurement ... lead the assessment of supplier relationship health across all R&D functions ( Clinical , Pre- Clinical and Discovery Research) for selected preferred suppliers.… more
- Otsuka America Pharmaceutical Inc. (Baton Rouge, LA)
- The Associate Director of Regulatory Intelligence leads the collection and dissemination of regulatory intelligence and collaborates with SMEs to interpret the ... + Ensure regulatory intelligence specialists have continued access to regulatory, clinical trial, and public domain information resources to identify relevant… more
- Lilly (Indianapolis, IN)
- … trial medicines, while also reducing costs and environmental impact. The Associate Director Small Molecule Process Engineering provides leadership and direction ... site evolves from a design concept to a GMP clinical trial site. **Key Responsibilities:** + Responsible for establishing...the technical agenda, site business plan objectives, and GMP Quality Plan objectives. + Identify, track, and report key… more
- Gilead Sciences, Inc. (Parsippany, NJ)
- …our day and improving the lives of patients for generations to come. As an Associate Director , Global Regulatory Affairs, you will act as the Regional Regulatory ... leaders and teams. + May participate on other Sub-teams (eg, Study Management, Clinical , Nonclinical, Biomarkers) or assign such to other colleagues and oversee and… more
- Bristol Myers Squibb (Indianapolis, IN)
- …team, RayzeBio aims to be the global leader in radiopharmaceuticals . The Associate Director of Validation is responsible for leading the validation function ... of validation personnel. + Collaborate closely with site leadership, engineers, QA/ Quality , and external vendors and contractors to ensure timely and compliant… more
- Omnicell (Coos Bay, OR)
- ** Associate Director , Specialty Pharmacy Operations** **SUMMARY** Responsible and accountable for all operational issues within a defined territory. Shall be ... (retail, specialty, or mail order). **Preferred:** + Multi-site management experience. + Clinical and Quality improvement experience. + Thorough knowledge of… more
- Stanford University (Stanford, CA)
- Associate Director , Outcomes and Development **School of Medicine, Stanford, California, United States** **New** Student Services Post Date 4 days ago ... MD, MS, MSPA, and PhD students; visiting MD students seeking clinical clerkships; postdoctoral scholars and medical fellows; and medical practitioners seeking… more
- AbbVie (Mettawa, IL)
- …YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description The Associate Director of International External Expert (EE) Engagement & ... to deliver compelling peer-to-peer education that clearly and effectively convey our clinical data + Provides direction to affiliates on optimal execution of… more