- Merck & Co. (North Wales, PA)
- …DescriptionUnder general supervision of an Executive Director/Senior Director, the Principal Scientist /Director is responsible for developing and implementing ... in accordance with domestic and international regulations and guidance.- The Principal Scientist is responsible for the leading the preparation and submission… more
- Merck & Co. (San Diego, CA)
- …team members.Our company is recruiting a highly motivated, detail-oriented Associate Principal Scientist with a passion for improving patient lives to support ... for drug treatment.- We seek a motivated, versatile, detail-oriented Associate Principal Scientist to join the Immunology Discovery and Translational Team located… more
- Merck & Co. (Rahway, NJ)
- …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 laboratory-based scientific role tasked with identifying, developing and deploying automation and… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionDevice Development Principal Scientist - Device Development Lead (Director Equivalent) Our company's Device Development (DD) Team designs, develops, ... and influence clinical and commercial combination product development and launches. Principal ResponsibilitiesLead and set direction for the device development… more
- Merck & Co. (Rahway, NJ)
- …and dedicated colleagues while developing and expanding your career.-- Director ( Principal Scientist)has primary responsibility for the planning and directing of ... clinical research activities involving new or marketed Oncology medicines. Our company's Oncology medicines span all phases of clinical development (pre-clinical to post-licensure). The Director will manage the entire cycle of clinical development, including:… more
- Merck & Co. (Rahway, NJ)
- …colleagues while developing and expanding your career.The Senior Director (Sr. Principal Scientist) has primary responsibility for the planning and directing ... clinical research activities involving new or marketed Oncology medicines. Our company's Oncology medicines span all phases of clinical development (pre-clinical to post-licensure). The Director will manage the entire cycle of clinical development, including… more
- 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 ... development projects.- Accountability predominantly includes the development and execution of statistical analysis and reporting deliverables (eg safety and efficacy analysis datasets, tables, listings, figures), the span of which range from individual… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionModeling and Informatics: Associate Principal Scientist, Computational Chemistry - Peptide Expert Position Description Our company is seeking a ... creative, self-motivated computational chemist with exceptional interpersonal and problem-solving skills to join the Modeling and Informatics group at our company headquarters in Rahway, NJ.We are expanding our capability in peptide computational chemistry to… more
- Merck & Co. (South San Francisco, CA)
- Job DescriptionOur Discovery Biologics group is seeking an Associate Principal Scientist with experience in biologics and data science to expand our abilities to ... design and engineer biotherapeutics.- We are building a department that directly integrates computational and wet-lab researchers with state-of-the-art automation to accelerate the discovery of novel biologics.- We are a highly diverse and collaborative group… more
- Merck & Co. (Rahway, NJ)
- …Our Quantitative Sciences team uses big data to analyze the safety and efficacy claims of our potential medical breakthroughs. We review the quality and reliability ... of clinical studies using deep scientific knowledge, statistical analysis and high-quality data to assist decision making in clinical trials.This position supports statistical programming activities for multiple and/or late stage drug clinical development… more
- Merck & Co. (Rahway, NJ)
- …(SPD) of your separation package, then you are no longer eligible for your separation benefits package. To discuss in more detail, please contact your HRBP or Talent ... Acquisition Advisor.Employees working in roles that the Company determines require routine collaboration with external stakeholders, such as customer-facing commercial, or research-based roles, will be expected to comply not only with Company policy but also… more
- Merck & Co. (North Wales, PA)
- …asset-specific translational deliverables & gaps.- Building testable hypothesis & forming BMx strategy: collaborate across different LFs, to formulate testable ... clinical and translational hypotheses; and develop clinical biomarker and translational research strategy to test the hypothesis.--Alignment, risk mitigation & strategy implementation:- align with asset development team strategy.- Build critical scientific… more
- Merck & Co. (North Wales, PA)
- …(SPD) of your separation package, then you are no longer eligible for your separation benefits package. To discuss in more detail, please contact your HRBP or Talent ... Job DescriptionThis position focuses on strategic activities impacting late-stage development therapeutic area (TA) projects to the direct benefit of project teams and the Biostatistics organization.The position is a key collaborator with internal and external… more
- Merck & Co. (Rahway, NJ)
- …(SPD) of your separation package, then you are no longer eligible for your separation benefits package. To discuss in more detail, please contact your HRBP or Talent ... Acquisition Advisor. Employees working in roles that the Company determines require routine collaboration with external stakeholders, such as customer-facing commercial, or research-based roles, will be expected to comply not only with Company policy but also… more
- WuXi AppTec (San Diego, CA)
- …of this position are to provide statistical consulting to clients in the biotech/pharmaceutical industry in their drug development programs with a focus on ... protocol/study design, analysis planning, and regulatory submission strategies. Provide statistical consulting to clinical study designReview study protocols and write statistical sectionsConduct sample size and power calculationsPropose randomization methods… more
- Lovelace Biomedical Research Institute (Albuquerque, NM)
- …revenue. Team Management & Mentorship: Manage and mentor a team of Principal Investigators and associated technical support staff. Foster an environment of ... innovation, collaboration and professional growth. Develop staffing plans and work with the Human Resources Department to design an overall talent strategy to achieve research goals.Resource Oversight: Oversee budgets, timelines and resource allocation with… more
- Merck & Co. (North Wales, PA)
- …dedicated colleagues while developing and expanding your career.The Clinical Director ( Principal Scientist) has primary responsibility for the planning and directing ... clinical research activities involving new Oncology medicines within an Asset team. Our Company's Oncology medicines span all phases of clinical development (pre-clinical to post-licensure). The Director will manage the entire cycle of clinical development,… more
- Eisai, Inc (Nutley, NJ)
- …and vendors, develops and maintains client relationships.As project lead/ principal investigator has project budget, deliverable and timeline responsibility; ... identifies scope expansion and need for project amendments.Mapping of payer/HTA engagement timelines for key global markets and coordinate stakeholders' engagement and responses to HTA and reimbursement challenges in close collaboration with Global, Regional,… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Senior Clinical Director (Sr. Principal Scientist) has primary responsibility for the strategic planning and directing clinical research ... activities involving investigational compounds in Immunology. With a focus on late-stage development, the Senior Clinical Director will manage the entire cycle of clinical development, including determination of appropriate disease indications to pursue and… more
- Daiichi Sankyo, Inc. (Nashville, TN)
- …experience in Oncology, clinical research and medical education preferred Principal MSL/Associate Director MSLExperience Qualifications:5 or More Years' experience ... including medical & scientific affairs, clinical practice, research, academic or US managed markets preferredPrevious experience in Oncology, clinical research and medical education preferred Must have a valid driver's license with a driving record that meets… more
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