• Insmed Incorporated (NJ)
    …other, and for the future of science, we're in. Are you?About the Role:The Director of Clinical Supply Chain Operations is responsible for leading global demand ... developing and executing strategic plans for production, packaging, distribution, and clinical supply budgeting. The Director provides strategic leadership for… more
    HireLifeScience (11/01/25)
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  • Merck & Co. (Rahway, NJ)
    …program cost estimates requested by Product Development Teams. Responsible for authoring clinical supply documentation in support of labeling and packaging ... approach to identify process inefficiencies, develop solutions, and drive continuous improvement initiatives within the clinical supply planning function. Proven… more
    HireLifeScience (10/30/25)
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  • Insmed Incorporated (NJ)
    …compliant state throughout their lifecycle a plus .Familiarity with validation of documentation , audit readiness, and continuous improvement of CSV processes. ... compliance with GxP regulations and industry standardsFamiliarity with validation of documentation , audit readiness, and continuous improvement of CSV processes… more
    HireLifeScience (11/01/25)
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  • Formation Bio (New York, NY)
    …policies for upfront license revenue recognition, and milestone treatment Partners with Director of Accounting, R&D, FP&A, and clinical operations to ensure ... than the industry can progress because of the high cost and time of clinical trials. Recognizing that this development bottleneck may ultimately limit the number of… more
    HireLifeScience (10/25/25)
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  • Merck & Co. (Rahway, NJ)
    …enables gain of critical internal experience during scale-up of clinical supplies manufacturing, demonstration of new manufacturing technology/processes, training ... operations, process development activities, compliance investigations/change management, authoring of GMP documentation , and lead other staff in the pilot plant as… more
    HireLifeScience (10/30/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …areas centered around rare diseases and immune disorders. Job Summary: The Director of Data Management (DM) Reporting provides leadership in Data Management ... and external stakeholders to oversee the development and delivery of clinical data programming, reporting, data visualizations, external data acquisition and… more
    HireLifeScience (10/27/25)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    About the Department The Clinical , Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... for a living. Are you ready to make a difference? The Position The Director Medical Review oversees a team of Medical Reviewers responsible for Medical Assessment of… more
    HireLifeScience (10/28/25)
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  • Daiichi Sankyo, Inc. (Bernards, NJ)
    …Key Quality Indicators (KQIs). Identify and drive initiatives for continuous quality improvement .Deputize for the Sr. Director , Medical Affairs QA as needed. ... centered around rare diseases and immune disorders. Job Summary: Reporting to the Sr. Director , Medical Affairs QA, the Director of Medical Affairs QA is… more
    HireLifeScience (09/03/25)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    About the Department The Clinical , Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... and Compliance, Global Safety, and centralized teams (eg, Training and Documentation , Quality, Supplier and Contract Management and Digital Enablement). This role… more
    HireLifeScience (10/28/25)
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  • CoxHealth (Lake Spring, MO)
    …to work with others and communicate effectively ▪ Ability to build presentations/present Clinical Documentation Improvement to providers fluently ▪ Ability ... to work with others and communicate effectively ▪ Ability to build presentations/present Clinical Documentation Improvement to providers fluently ▪ Ability… more
    Talent (10/15/25)
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  • Insmed Incorporated (NJ)
    …and for the future of science, we're in. Are you?About the Role:The Sr. Director CMC QA will lead QA CMC oversight for drug products, biologics, and combination ... and internal standards.Serve as the Quality lead for GMP activities supporting clinical trial materials, including DS/DP used in early and late-phase studies.Oversee… more
    HireLifeScience (08/27/25)
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  • Insmed Incorporated (Minneapolis, MN)
    …the future of science, we're in. Are you?About the Role:The Associate Director Medical Science Liaison will develop and maintain professional relationships with ... assigned budget parametersIs accountable for the accurate and timely documentation of all activitiesIdentify Medical Experts, consultants, investigators, and… more
    HireLifeScience (09/05/25)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    … operations, medical affairs, and regulatory affairs Maintain training assignments on clinical research documentation , regulatory requirements, Good Clinical ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo...regulated environment. Relationship This job reports to the Senior Director of the GxP Compliance & Technical Operations or… more
    HireLifeScience (10/28/25)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    …of GxP documentation to verify compliance and identify areas for improvement or corrective actions Collaborate with cross-functional teams to ensure that GxP ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo...against established metrics Prepare and present regular reports on documentation compliance, audit results, and improvement initiatives… more
    HireLifeScience (10/28/25)
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  • Bethesda Health (Kirkwood, MO)
    …Summary Provides management oversight for multiple nursing neighborhoods and assists the Director of Nursing as needed. Acts as a resource to staff regarding ... concerns and needs. Communicates events requiring administrative attention to the Director of Nursing. Recommends corrective action when problems are identified,… more
    Talent (11/01/25)
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  • Novo Nordisk Inc. (Plainsboro, NJ)
    About the Department The Clinical , Medical and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the ... with SDEA requirements. Relationships This position reports to the Associate Director , Safety Contracts & Supplier Management. This position works closely with… more
    HireLifeScience (10/29/25)
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  • Boost Home Health (Frisco, TX)
    …and enforce Boost HHC policies to ensure regulatory compliance and accurate clinical documentation . Engage in performance improvement initiatives and ... continuous improvement . Lead QA/PI activities to maintain and elevate clinical standards. Manage patient care assignments and oversee staff performance, stepping… more
    Upward (08/04/25)
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  • Executive Care (Leesburg, VA)
    …(EHC) Organization (HCO). This role ensures regulatory compliance, drives quality improvement initiatives, and provides leadership support across clinical , non- ... Reporting to the Governing body headed by the President and CEO, the Director of Operations and Administration is a pivotal leadership role responsible for… more
    Upward (08/04/25)
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  • Jobleads-US (Roseville, CA)
    …of the facility's educational programs for all employees and quality assurance and improvement in the facility. Director of Staff Development Qualifications A ... and supervision of the Administrator and through consultation and cooperation with the Director of Nurses, the Director of Staff Development Registered Nurse… more
    Appcast IO CPC (10/28/25)
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  • Jobleads-US (Baltimore, MD)
    …upon campus. Your recruiter will advise accordingly. The pre-employment physical for clinical areas may require documentation of immune status against Rubella, ... Overview Johns Hopkins University seeks an Executive Director HR - Total Rewards to provide strategic leadership for the University's compensation and benefits… more
    Appcast IO CPC (10/31/25)
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