- Merck (Rahway, NJ)
- …and vaccine arenas. Specifically, CET is seeking an Associate Principal Scientist specializing in bioprocessing purification technologies for multiple ... **Job Description** **Associate Principal Scientist - Continuous & Expression...tools aimed at improving production processes in our company's drug candidate pipeline. Knowledge of intensified unit operations such… more
- Merck (Rahway, NJ)
- …and routes of administration, including inhalation, implantation, and injection. The Associate Principal Scientist will lead the definition and execution of ... which focuses on the design, development, and commercialization of novel biologic/ drug / vaccine -device combination products for safe and effective delivery to… more
- Merck (Rahway, NJ)
- **Job Description** **Associate Principal Scientist - Device Technical and Engineering Lead (Associate Director Equivalent)** _Our company's Device Product & ... Process Development (DPPD) Team designs, develops, and commercializes novel biologic/ drug / vaccine - device enabled combination products to achieve safe and… more
- Merck (Rahway, NJ)
- …teams. + Lead, develops, coordinates, and provides biostatistical support for related drug / vaccine projects in Late Development Statistics. + Lead the ... clinical trials, and in coordinating the statistical activities for clinical drug / vaccine projects. + Interacts with Academic Research Organization (ARO),… more
- Merck (Rahway, NJ)
- …supports statistical programming activities for multiple and/or late stage drug / vaccine clinical development projects. Accountability predominantly includes the ... the activities of a programming team. + US and/or worldwide drug or vaccine regulatory application submission experience at the leadership level including the… more
- Pfizer (Pearl River, NY)
- **ROLE SUMMARY** The primary purpose is to serve as a Clinician within a Pfizer vaccine development program. This role may serve as a clinical lead for one or more ... clinician medical monitor may delegate these responsibilities to the study clinician scientist identified in the SSRP. The specific components of safety data review… more