• Merck & Co. (Rahway, NJ)
    …for the benefit of patients and global human health.Responsibilities: The Senior Statistical Programmer, Submission Data Standards Quality Management (SDS QM), ... provides oversight and quality management of submission data standard deliverables for world-wide regulatory application submissions of drug and vaccine clinical development projects. Accountability predominantly includes submission data standards planning… more
    HireLifeScience (07/29/25)
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  • Merck & Co. (Rahway, NJ)
    …of clinical protocol(s) . This may include: Serving as the lead clinical scientist on the clinical trial team. Leading medical monitoring team in review and ... interpretation -of clinical data/medical protocol deviations in collaborations with the Clinical Director. Other responsibilities include: Collaborating cross-functionally in the development of Protocol and related study materials (e . g . , ICF documents/… more
    HireLifeScience (07/24/25)
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  • Insmed Incorporated (San Diego, CA)
    …to keep you challenged and engaged. If you are a driven and astute scientist who is motivated to bring life-changing medicine to patients, then this is the ... role for you.ResponsibilitiesExecute technical strategies for purification process development to support pre-clinical and clinical programs at all development stages, including process development, optimization, technology transfer, and process… more
    HireLifeScience (07/14/25)
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  • Twist BioScience (South San Francisco, CA)
    Senior / Staff Bioinformatics Production Scientist (Hybrid in South San Francisco)Position OverviewWe are seeking a highly motivated, results-oriented, and ... to join our Bioinformatics and Analytics team as a Senior /Staff Bioinformatics Production Scientist . In this role, you will combine genomics expertise with… more
    HireLifeScience (06/17/25)
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  • Merck & Co. (South San Francisco, CA)
    Job Description Senior Principal Scientist Translational Medicine, Immunology Translational Medicine in our Research & Development Division is responsible for ... the Immunology Therapeutic Area Lead in Translational Medicine.Primary responsibilities for the Senior Principal Scientist include the following:Key member of an… more
    HireLifeScience (07/30/25)
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  • Tris Pharma (Monmouth Junction, NJ)
    …New Jersey, Tris has an immediate opening for a Method Validation R&D Senior Scientist ISummary:The Method Validation (MV) Research and Development (R&D) ... Senior Scientist I, under minimal guidance, performs analytical method validations and release/stability raw materials, in process (IP), finished products (FP)… more
    HireLifeScience (07/30/25)
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  • Merck & Co. (Rahway, NJ)
    …state-of-the-art technology and applying rigorous scientific and ethical standards.The Senior Director has primary responsibility for the planning and directing ... (pre-clinical to post-licensure). With a focus on late-stage development, the Senior Director will manage the entire cycle of clinical development, including… more
    HireLifeScience (07/30/25)
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  • Merck & Co. (Rahway, NJ)
    …technical responsibility and leadership of internal and external work.The Senior Scientist , Engineering position leverages scientific/technical experience to ... lab scales in addition to technology transfer to commercial manufacturing facilities. The scientist will be expected to exhibit a mindset of safety and quality… more
    HireLifeScience (07/26/25)
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  • Merck & Co. (Rahway, NJ)
    …bioprocessing to join Biologics Process Research & Development (BPR&D) as a Senior Principal Scientist .BPR&D within Research Laboratories is committed to rapidly ... with the scientific community to influence the field.As a Senior Principal Scientist , you will drive various strategic initiatives and translate strategies… more
    HireLifeScience (07/24/25)
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  • Aequor (South San Francisco, CA)
    …MCWB workflows. The overarching concept involves Senior Staff initiating an MCWB routine and then passing it on to the Associate Scientist for regular execution ... Cell Biology, Molecular Biology, or a related field. An Associate Scientist With a background in Immunology, Pharmacology, Cell Biology, Molecular Biology,… more
    HireLifeScience (08/01/25)
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  • Merck & Co. (North Wales, PA)
    …execution of clinical protocol(s). This may include:Serving as the lead clinical scientist on the clinical trial team.Leading medical monitoring team in review and ... interpretation of clinical data/medical protocol deviations in collaborations with the Clinical Director.Other responsibilities include:Collaborating cross-functionally in the development of Protocol and related study materials (eg, ICF documents /… more
    HireLifeScience (07/26/25)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionAs a Senior Engineer in Device Design and Process Development group, you will be part of our Research & Development team that designs and develops ... benchtop/low-volume to high-volume clinical and commercial assembly equipment and processes for medical devices/drug delivery systems. Reporting to the Director responsible for this area, you will partake in medical device assembly and process development… more
    HireLifeScience (07/22/25)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionDevice Development Associate Principal Scientist - Development Strategy, Design Controls(Associate Director Equivalent) Our company's Device ... formal authority; ability to influence and present ideas to senior leadershipExcellent communication, presentation, negotiation, project management, and organizational… more
    HireLifeScience (07/30/25)
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  • Merck & Co. (Upper Gwynedd, PA)
    …Principal Scientist , CMC, R4 - Pharm Pre-approval Reporting to the Sr Director/Director/Principal Scientist / Sr Principal Scientist in Pre-approval ... Pharmaceutical CMC is responsible for developing and implementing CMC regulatory strategies for our company's pharmaceutical pipeline products in accordance with global regulations and guidances, and is-responsible for the preparation and submission of CMC… more
    HireLifeScience (07/19/25)
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  • Merck & Co. (Rahway, NJ)
    …certifications, experience, skills, geographic location, government requirements, and business or organizational needs. The successful candidate will be eligible for ... Job DescriptionResponsibilities:Provide high quality statistical programming deliverables for global stakeholders in Early Development Statistics and PK/PD Modeling and Simulation spanning all therapeutic areas except early oncology.Gather and interpret user… more
    HireLifeScience (07/23/25)
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  • Merck & Co. (Rahway, NJ)
    …:Develops, coordinates, and provides biostatistical support for related drug/vaccine projects under supervision in Late Development Statistics. --Interacts with ... Clinical, Regulatory, Statistical Programming, Data Management and other company Research Laboratories Scientists in designing and analyzing clinical trials, and in coordinating the statistical activities for clinical drug/vaccine projects.The incumbent may… more
    HireLifeScience (07/16/25)
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  • Merck & Co. (Rahway, NJ)
    Scientist position available at its Rahway, New Jersey research facility. The Principal Scientist is a senior scientific role tasked with working closely with ... the group Director to define group strategy and to lead a team of scientists in solving complex analytical problems at the interface of biology, chemistry, and lab informatics disciplines to enable development of biologics pipeline.We are looking for a team… more
    HireLifeScience (07/24/25)
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  • Merck & Co. (Rahway, NJ)
    …administration including inhalation, implantation, and injection.--This position serves as a senior individual contributor who will be responsible for applying deep ... device and combination product strategies and development efforts in senior -level governance reviews.-Furthermore, the successful candidate will spend time mentoring… more
    HireLifeScience (07/29/25)
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  • Merck & Co. (Rahway, NJ)
    Job DescriptionRole SummaryUnder the guidance of a senior leader, an Associate Principal Scientist /Associate Director, has primary responsibility for ... planning/managing real world and economic evidence activities for in-line and pipeline immunology products to meet the value evidence needs of clinicians, payers, policymakers, HTA/reimbursement agencies, and health systems globally.Types of studies executed… more
    HireLifeScience (07/23/25)
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  • Merck & Co. (Rahway, NJ)
    …to join Biologics Process Research & Development (BPR&D) as a Principal Scientist .BPR&D within Research Laboratories is on a mission to rapidly deliver diverse ... and engage with the scientific community to influence the field.As a Principal Scientist you will have the opportunity to influence the future direction of Upstream… more
    HireLifeScience (07/17/25)
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