• Genmab (NJ)
    …feel like a fit? Then we would love to have you join us!Role:The Associate Director acts as a statistical expert supporting the clinical development of compounds as ... trial responsible statistician with responsibilities as described below. The Associate Director contributes to clinical development strategies and plans.Responsibilities:Compound/Indication… more
    HireLifeScience (07/30/25)
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  • Eisai, Inc (Nutley, NJ)
    …therapeutic area.Under the direction of the Vice President, Medical Affairs the Associate Medical Director is responsible for working with key stakeholders to ... assigned product(s) and prepare progress updates as needed.Participate in the design strategies, planning and implementation of Phase IV clinical development… more
    HireLifeScience (08/15/25)
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  • Insmed Incorporated (NJ)
    …and for the future of science, we're in. Are you?About the Role:The Associate Director of Biostatistics is responsible for the statistical aspects for complex ... of cross functional teams, accountable for statistical aspects of statistical design , study setup, execution, analysis and reporting of clinicals.Manage the… more
    HireLifeScience (09/15/25)
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  • Insmed Incorporated (NJ)
    …and for the future of science, we're in. Are you?About the Role:The Associate Director, Clinical Research Scientist will support and work predominately with the ... aspects and stages of the protocol development and execution from study design planning through final reporting of result.Provide scientific input and review of… more
    HireLifeScience (09/12/25)
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  • Merck & Co. (Rahway, NJ)
    …and scaling-up the formulation, device, and manufacturing process. Driving drug product design from the bench top to the Good Manufacturing Practice (GMP) ... results - Can independently execute formulation and process development activities using Design of Experiment s for new chemical entities or life cycle management… more
    HireLifeScience (09/17/25)
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  • Merck & Co. (North Wales, PA)
    …trials to world-wide regulatory application submissions and post marketing support.- Design and maintain statistical databases that support multiple stakeholder ... to be programmed; Understanding of statistical terminology and concepts; design and develop complex programming algorithms.Ability to anticipate stakeholder and… more
    HireLifeScience (09/03/25)
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  • Merck & Co. (Rahway, NJ)
    …submissions and post marketing support.The incumbent is responsible for the design and maintenance of statistical datasets that support multiple stakeholder groups ... process compliance.Strategic thinking - ability to turn strategy into tactical activities; design of statistical databases with the end in mind that optimize… more
    HireLifeScience (09/30/25)
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  • Lupin Pharmaceuticals (Coral Springs, FL)
    …compliance. ResponsibilitiesEssential Duties and Responsibilities Clinical Development: Design and execute clinical trials for respiratory products, ... ensuring compliance with regulatory requirements.Collaborate with cross-functional teams to develop study protocols, analyze trial data, and manage trial progress. Medical Monitoring: Provide medical oversight during clinical trials to ensure participant… more
    HireLifeScience (09/15/25)
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  • Schaeffler (Danbury, CT)
    Engineer Associate - Mechanical Design Engineering Location: Danbury, CT, US, 6813 Job Requisition ID: 37981 Schaeffler is a dynamic global technology company ... + Extensive knowledge of bearing manufacturing practices + 2+ years of design experience in aerospace or space manufacturing **Our Offering** + Comprehensive… more
    DirectEmployers Association (10/25/25)
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  • Stellant Systems (Torrance, CA)
    …authorized by Engineering Change Notices. + Check the accuracy of other mechanical designer 's work. **Qualifications** + Associate 's degree and a minimum of 8 ... **Overview** **Job Title: Senior Design Specialist** **Job Location: Torrance, CA** **Salary: $115,000-$130,000/yr DOE** Stellant Systems currently has an… more
    DirectEmployers Association (10/01/25)
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