- Merck & Co. (Rahway, NJ)
- …department of our Research & Development Division is seeking applicants for an Associate Principal Scientist position available at its Kenilworth, New ... Jersey research facility.- The Associate Principal Scientist is a...program deadlines.Authoring and reviewing internal technical reports, sections of regulatory filings (eg, IND, BLA) and external scientific publications.Experience… more
- Merck & Co. (Rahway, NJ)
- …products and processes are developed in accordance with applicable regulatory , quality, company, and customer requirements.-This position will lead cross-functional ... and influence clinical and commercial combination product development and launches. Principal ResponsibilitiesLead and set direction for the device development… more
- Merck & Co. (Rahway, NJ)
- … Principal Scientist , Small Molecule Research & DevelopmentIn your role as Associate Principal Scientist , you will be part of a team developing ... imaging tools, and data analysis. You would also contribute towards regulatory submissions to enable clinical trials. Your main responsibilities, which are… more
- Organon & Co. (Jersey City, NJ)
- **Job Description** **The Position** The Associate Principal Scientist is responsible for developing and implementing Regulatory CMC strategies for ... with global regulations and guidance's, and Company procedures. The Associate Principal Scientist will lead...products and be accountable for the delivery of all regulatory milestones for assigned products through the product lifecycle.… more
- L'Oreal USA (Clark, NJ)
- …(https://careers.loreal.com/en\_US/content/Home) / Job Search (https://careers.loreal.com/en\_US/jobs/SearchJobs) / 178053 Associate Principal Scientist , ... NJ, New Jersey Research & Innovation Full - Time 15-Apr-2024 Position Title: Associate Principal Scientist , Advertising Claims Substantiation Location :… more
- L'Oreal USA (Clark, NJ)
- …(https://careers.loreal.com/en\_US/content/Home) / Job Search (https://careers.loreal.com/en\_US/jobs/SearchJobs) / 176296 Associate Principal Scientist , ... NJ, New Jersey Research & Innovation Full - Time 26-Mar-2024 Position Title: Associate Principal Scientist , Ingredients Innovation Advanced Research Location… more
- Merck (Rahway, NJ)
- **Job Description** Associate Principal Scientist , Small Molecule Research & Development In your role as Associate Principal Scientist , you will ... imaging tools, and data analysis. You would also contribute towards regulatory submissions to enable clinical trials. Your main responsibilities, which are… more
- Merck (Rahway, NJ)
- …department of our Research & Development Division is seeking applicants for an Associate Principal Scientist position available at its Kenilworth, New ... Jersey research facility. The Associate Principal Scientist is a...+ Authoring and reviewing internal technical reports, sections of regulatory filings (eg, IND, BLA) and external scientific publications.… more
- Merck (Rahway, NJ)
- …we collaborate to discover the next medical breakthrough. **Position Description:** The Associate Principal Scientist Statistical Programming leads the ... art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for… more
- Merck (Kenilworth, NJ)
- …experienced individual to join our Downstream Process Development and Engineering group as an Associate Principal Scientist . In this role, you will work with ... yield, robust and scalable processes. + Responsible for process characterization and regulatory filings to ensure a smooth and clear path to successful… more
- Merck (Rahway, NJ)
- …ensure products and processes are developed in accordance with applicable regulatory , quality, company, and customer requirements. This position will lead ... and influence clinical and commercial combination product development and launches. ** Principal Responsibilities** Lead and set direction for the device development… more
- Merck (Rahway, NJ)
- …art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for ... the span of which range from individual clinical trials to world-wide regulatory application submissions and post marketing support. The incumbent is responsible for… more
- Pfizer (Pearl River, NY)
- …and publications. + May contribute budget execution of protocols. **Interact with regulatory authorities, key opinion leaders, and principal investigators:** + ... clinician medical monitor may delegate these responsibilities to the study clinician scientist identified in the SSRP. The specific components of safety data review… more
- Pfizer (Pearl River, NY)
- …for the on-time and within-budget execution of protocols **Interact with regulatory authorities, key opinion leaders, and principal investigators.** + ... expertise to steer clinician medical monitors, clinician clinical scientists, clinical scientist leads, and other clinical staff members. The clinician medical… more
- Pfizer (Pearl River, NY)
- …and publications. + May contribute budget execution of protocols **Interact with regulatory authorities, key opinion leaders, and principal investigators:** + ... clinician medical monitor may delegate these responsibilities to the study clinician scientist identified in the SSRP. The specific components of safety data review… more
- Merck (Rahway, NJ)
- …while developing and expanding your career. The Senior Clinical Director (Sr. Principal Scientist ) has primary responsibility for the planning and directing ... of clinical development, including: study design, placement, monitoring, analysis, regulatory reporting, and publication. **Specifically, the Senior Director may be… more
