- Merck & Co. (Rahway, NJ)
- …and in the preparation of study documents for submission to regulatory agenciesExcellent verbal communication and presentation skills required; required to represent ... the group in internal meetings, in meetings with regulatory agencies and in scientific meetingsWorking knowledge of standard computer software applications for… more
- Merck & Co. (North Wales, PA)
- …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 & 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. (North Wales, PA)
- …art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for ... with Meta Data Repositories.United States and/or worldwide drug or vaccine regulatory application submission experience at the leadership level including the… more
- Merck & Co. (North Wales, PA)
- …dataProduce tables and graphics for inclusion in study reports and regulatory submissionsEnsure programmatic traceability from data source to modeling resultSupport ... programming deliverablesproduce SAS transport files and associated documentation for regulatory submissionsRepresent statistical programming on process improvement activities. Education… more
- Merck & Co. (North Wales, PA)
- …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 & Co. (North Wales, PA)
- …and dedicated colleagues while developing and expanding your career.The Clinical Director ( Principal Scientist ) has primary responsibility for the planning and ... of clinical development, including: study design, placement, monitoring, analysis, regulatory reporting, and publication.-Specifically, the Director may be responsible… 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 Be… more
- Fidelity TalentSource LLC (Boston, MA)
- …related technical fields.5+ years of prior work experience as a Data Scientist .Hands-on experience in most of the following: Knowledge Graphs, Graph Learning, ... best of working offsite with maximizing time together in person to meet associate and business needs. Currently, most hybrid roles require associates to work onsite… more
- George Washington University (Rockville, MD)
- …at: www.bsc.gwu.edu.The Biostatistics Center is seeking a regular full-time Sr. Research Scientist to work for a research team serving as the Coordinating Center ... Study. Position will serve as a Data Engineer and Scientist role and leads the design and development for...at a level functioning similar to that of an Associate or Full Professor. Using broad familiarity with a… more
- Fidelity TalentSource LLC (Boston, MA)
- Job Description:The RoleYou are a seasoned scientist with a deep understanding of GenAI, and a burning desire to unlock its mysteries in the context of a ... earnings notes, spreadsheet models, prospectuses, loan indentures, news reports, regulatory filings. It will support the deployment of personalized assistants… more
- Organon & Co. (Plymouth Meeting, PA)
- **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 (West Point, PA)
- **Job Description** We are seeking an Associate Principal Scientist to join our Vaccine Analytical Research and Development Separations and Biochemical ... lead assay development, drive scientific contributions at program levels, mentor scientist , and engage with product teams to characterize vaccines supporting process… 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
- IQVIA (Durham, NC)
- We are seeking an ** Associate Principal Scientist , Reagents** to join Q2 Solutions, IQVIA's laboratory business in **Durham NC.** We hire passionate ... as we transform and accelerate research and development. The ** Associate Principal Scientist , Reagents** is...job area. + Basic knowledge of requirements under relevant regulatory standards for the assigned work area. + Expertise… more
- Merck (South San Francisco, CA)
- …Our Research & Development Division located in South San Francisco is seeking an Associate Principal Scientist with strong expertise in complex cellular ... biologic preclinical candidates targeting cardiovascular and metabolic disorders. In addition, the Associate Principal Scientist will participate in business… 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 (West Point, PA)
- …assays and test pre-clinical and/or clinical samples as needed. The responsibilities of the Associate Principal Scientist will be to work collaboratively in ... reports, and to participate on cross-functional teams. . Responding to regulatory authorities pertaining to bioanalytical strategy and execution. . Serve as… more
