- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Associate Principal Programmer leads the statistical programming activities for multiple and/or large/complex late stage drug/vaccine clinical ... 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
- Merck & Co. (Rahway, NJ)
- …Development department of our Research Laboratory Division is seeking applicants for an Associate Principal Scientist position within the Automation group, ... available at its Rahway, New Jersey research facility.- The Associate Principal Scientist is a...well as data analysis and statistics Working knowledge of Regulatory Good Practices (GxP) with regards to laboratory experimentation… more
- Merck & Co. (Rahway, NJ)
- …enhancements, next generation process development, and authoring of regulatory submissions.Under the general scientific and administrative department direction ... Represents functional area on cross-functional and cross-divisional teams.Authors required regulatory and technical documentation.- Ensures that processes are developed… more
- 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)
- … 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
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Senior Clinical Director (Sr. Principal Scientist ) has primary responsibility for the strategic planning and directing clinical research ... pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication. Specifically, The Senior Clinical Director May… 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) / 180058 Associate Principal Scientist , ... Research & Innovation Full - Time 21-May-2024 Position Title: Associate Principal Scientist , Hair Color...regional hubs, 14 evaluation centers, and 49 scientific and regulatory departments. Our employees represent over 60 nationalities and… 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)
- …Development department of our Research Laboratory Division is seeking applicants for an Associate Principal Scientist position within the Automation group, ... available at its Rahway, New Jersey research facility. The Associate Principal Scientist is a...as data analysis and statistics + Working knowledge of Regulatory Good Practices (GxP) with regards to laboratory experimentation… 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 (Rahway, NJ)
- …motivated and energetic individual to join our Biologics Process Development Department as Associate Principal Scientist . In this role, the successful ... and scalable cell culture processes. + Responsible for process characterization and regulatory filing activities to ensure a smooth and clear path to successful… more
- Merck (Rahway, NJ)
- **Job Description** As an Associate Principal Scientist , Biomarker Operations, Companion Diagnostics within the Biomarker Operations team, your primary ... and companion diagnostic partners: You will work closely with scientists, regulatory experts, and clinical and biomarker operations teams to ensure alignment… more
- Merck (Rahway, NJ)
- …process enhancements, next generation process development, and authoring of regulatory submissions. Under the general scientific and administrative department ... functional area on cross-functional and cross-divisional teams. + Authors required regulatory and technical documentation. Ensures that processes are developed and… 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
- Merck (Rahway, NJ)
- **Job Description** The **Senior Clinical Director (Sr. Principal Scientist )** has primary responsibility for the strategic planning and directing clinical ... pursue and subsequent study design, initiation, execution, monitoring, analysis, regulatory filing, and publication. **Specifically, The Senior Clinical Director May… more
