• Aequor (Thousand Oaks, CA)
    …for an enthusiastic, highly motivated, and team-oriented scientist for the position of Associate Scientist or Senior Associate Scientist . In this ... role, the scientist will serve as member of Drug Product development teams, providing hands-on formulation and process expertise during the development of clinical and commercial formulations for solid oral dosage forms. The individual will design and… more
    HireLifeScience (03/23/24)
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  • Aequor (South San Francisco, CA)
    …are: A basic level of pathology/lab experience and Image Analysis Experience. is seeking an Associate Scientist / Scientist to work in the Pathology Lab in ... Safety & Bioanalytical Sciences Department in South San Francisco, CA. The Associate Scientist / Scientist will develop and implement image analysis… more
    HireLifeScience (03/08/24)
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  • Merck & Co. (Rahway, NJ)
    …that are deployed in support of clinical trials. The candidate for this Associate Principal Scientist position should have strong technical expertise in ... molecular biology and tissue biomarker assessment and should have a strong interest in lab-based pathology assay work. In addition, the successful candidate should have the desire to collaborate closely with out-sourcing partners on the scientific oversight of… more
    HireLifeScience (03/27/24)
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  • Merck & Co. (North Wales, PA)
    …Develop and validate global programming standards and tools for the production of Study Data Tabulation Model (SDTM) datasets.Design and develop complex programming ... Job DescriptionIn BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our company's renowned Research and Development division, quantitative scientists, in partnership with other subject matter experts, apply state-of-the… more
    HireLifeScience (03/27/24)
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  • Aequor (Thousand Oaks, CA)
    …include: - Supporting a small molecule hit validation and characterization using cell/molecular biology technologies to Client Client molecular glues as a new ... therapeutic modality based on targeted protein degradation. - Follows established experimental design and protocols, as well as routine tasks and studies, to obtain reproducible and reliable results under supervision. - Plan, monitor or conduct experiments,… more
    HireLifeScience (03/27/24)
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  • Merck & Co. (North Wales, PA)
    …the clinical/scientific execution of clinical protocol(s).Serves as the lead clinical scientist on the clinical trial team.Collaborates with the Medical Writer on ... clinical/scientific and regulatory documents.Partners with Study Manager on study deliverables.Participates in the set up and design during study start up (eg, database set up)Lead medical monitoring team in review and interpretation of clinical data/medical… more
    HireLifeScience (03/22/24)
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  • Merck & Co. (Rahway, NJ)
    …for innovation and interest in contributing to upstream and/or downstream bioprocessing.As an Associate Scientist in BPR&D you will work with a highly ... Job DescriptionBiologics Process R&D Associate ScientistOur Research Scientists are our Inventors.- Using innovative thinking, state-of-the-art facilities, and… more
    HireLifeScience (03/21/24)
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  • Catalent (St. Petersburg, FL)
    Associate Scientist II, Analytical Research & Development Position Summary Catalent is a global, high-growth, public company, and a leading partner for the ... regulatory requirements, and St. Petersburg's Quality departmental policies. Once trained, the Associate Scientist II will independently test raw materials to… more
    HireLifeScience (03/15/24)
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  • Insmed Incorporated (San Diego, CA)
    …York™, and Best Workplaces for Millennials™ lists.OverviewInsmed is seeking a scientist with significant experience with mouse vivarium experiment management and ... execution. This scientist will be responsible for execution of preclinical mouse...genotyping, dosing, functional analysis, and tissue collection. Additionally, the scientist will document his/her methods and studies, and participate… more
    HireLifeScience (03/12/24)
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  • Merck & Co. (North Wales, PA)
    …Essential functions include, but are not limited to:Performs primary medical review-of serious adverse experience reports and other AE reports of interest to monitor ... and describes the safety profile of assigned products; taking an active role in the oversight and development of- pharmacovigilance and risk management plans with direction/guidance from the Clinical Safety and Risk Management (CSRM) team.Assists the CSRM team… more
    HireLifeScience (03/23/24)
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  • Aequor (Thousand Oaks, CA)
    …see resumes first will shortlist EOD Friday 3/15 Global Periodic Reports Scientist Organization Global Patient Safety & Pediatrics Group Purpose Group is accountable ... regulatory authority experience in a research and development setting OR Associate 's degree and 12years of pharmaceutical, biotech or regulatory authority experience… more
    HireLifeScience (03/14/24)
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  • Merck & Co. (North Wales, PA)
    Job DescriptionOur Biomarker Operations team is seeking an Associate Principal Scientist in Genomics Policy to help drive innovative biomarker research across ... the company's portfolio.- The goal of the organization is to ensure compliant utilization of clinical participant biospecimens to answer scientific questions across the company's pipeline, with an emphasis on the Oncology pipeline and innovations to improve… more
    HireLifeScience (02/21/24)
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  • Merck & Co. (North Wales, PA)
    …:This position provides high quality statistical programming analysis and reporting deliverables for global PK modeling and simulation stakeholders Oncology ... therapeutic area.- The programming analyst will gather and interpret user requirements, retrieve the required data, transform the data into modeling-ready analysis datasets, and develop tables and figures according to the modeling analysis plans.-- The… more
    HireLifeScience (03/12/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …research areas centered around rare diseases and immune disorders.Summary The Associate Director, RACMC Portfolio Products, will be responsible for regulatory CMC ... (Chemistry, Manufacturing, and Controls) activities of the portfolio small molecule and biological drug products consistent with the company goals; specifically, for the life-cycle management of NDAs/BLAs. This individual will be responsible for working on… more
    HireLifeScience (03/01/24)
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  • Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …Join a Legacy of Innovation 110 Years and Counting!Daiichi Sankyo Group is dedicated to the creation and supply of innovative pharmaceutical therapies to improve ... standards of care and address diversified, unmet medical needs of people globally by leveraging our world-class science and technology. With more than 100 years of scientific expertise and a presence in more than 20 countries, Daiichi Sankyo and its 16,000… more
    HireLifeScience (03/01/24)
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  • Merck & Co. (North Wales, PA)
    …all of our company's therapeutic areas except early oncology. -The Associate Principal Statistical Programmer will gather and interpret user requirements for ... which are not currently available through commercial software packages. The Associate Principal Programmer will be a key collaborator with statisticians, modelers,… more
    HireLifeScience (02/24/24)
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  • 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 ... 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
    HireLifeScience (02/27/24)
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  • Shimadzu Scientific Instruments (Los Angeles, CA)
    …travel by air and drive as required. (Daily) Assist with training Associate MS Support Specialists. (Weekly) Assist with Demonstrations. (Weekly) SCOPE: This ... position's primary focus is to provide LC-MS technical expertise for the selling effort of the assigned region(s) to meet business goals. KNOWLEDGE REQUIREMENTS: CASUAL WORKING THOROUGH ApplicationsTraining Methods Report Preparation Instrument Maintenance… more
    HireLifeScience (02/29/24)
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  • Lundbeck (San Diego, CA)
    …PREFERRED EDUCATION, EXPERIENCE AND SKILLS: Experience leading project teams Expertise in state-of-the-art cheminformatics systems and methods, including AI/ML ... Experience in hit triage, hit-to-lead chemistry, tool identification, and parallel synthesis Experience in CNS drug discovery Familiarity with chemical biology principles TRAVEL: Willingness/Ability to travel up to 10% domestically. International travel may be… more
    HireLifeScience (01/05/24)
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  • Merck & Co. (Rahway, NJ)
    …Description Role and Responsibilities: We are seeking an experienced talented scientist to join the Quantitative Pharmacology and Pharmacometrics - Immune/Oncology ... (QP2-IO) team in the role of Associate Director QP2-IO team is part of the Global...pharmacology and pharmacometrics of oncology drugs from post-PCC to registration. Associate Directors are emerging leaders in the field of… more
    HireLifeScience (03/26/24)
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