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The Associate Director, Long Range Supply and Capacity Planning Global Process Leader is responsible for E2E cross functional excellence in the Long-Range Supply and Capacity Planning pillar within the Biologics, Pharmaceuticals and Cell Therapy Commercial Business Units.
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Keywords: Biomedical, bmet, equipment technician, bmet 3, bmet iii, medical, medical device, princeton, contract, contract to hire, on site, onsite, maintenance, maintain, repair, calibrate, patient care, technical support, integration, oem, original equipment manufacturers, aem, alternative equipment maintenance, inspections, training, clinical, user operation, pre-purchase, health insurance portability, hipaa, joint commission, field, medical hardware, aami, diagnostic, health system.
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We are seeking motivated and qualified candidates to join our team in Princeton, New Jersey or Philadelphia, Pennsylvania as an environmental senior managing consultant or managing consultant with a focus on land use permitting for our site solutions (investigation and remediation) team.
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If KE Camps can meet your internship requirements, your on-site Camp Director will be your field supervisor and oversee your course work. Supervise daily swim time in a hands-on manner from within the water (lifeguard certification not required.
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Extensive knowledge of a broad array of systems including Clinical Trials Management System (CTMS); Risk Based Monitoring (RBM); Electronic Trial Master File (eTMF); Electronic Data Capture (EDC); Clinical Studies Operational Data Warehouse & Analytics; Site Training and Resource Management etc.
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Plan and host on-site wellness activities such as fairs, flu-shots, biometric screenings, massages etc. Support key compensation life cycle events, including annual salary increase planning, bonuses, LTI administration, and semi-annual promotion processes.
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The Assistant Director must also be experienced in software development methodologies, data security, project management principles, software quality assurance, applications governance & portfolio management, resource planning & allocation, and budget forecasting.
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Participate in system design consulting, platform management, and capacity planning. All applicants will be evaluated solely on the basis of their ability, competence and their proven capability to perform the functions outlined in the corresponding role.
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Safety management responsibilities required for clinical study program oversight inclusive of adverse event adjudication, MedDRA coding, and management of escalation of events to Complaints and reporting to ethics boards per their requirements.
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We are looking for an Analytical Development Scientist to join our team on-site in Hopewell, NJ. Ability to work on a computer for extended periods of time. This is a contracted role until 7/04/2025 with the potential to extend based on budgets and headcount.
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This role leads or supervises scenario planning, enrollment projections, study enrollment progress modeling, and site recommendations to accelerate study start-up and enrollment timelines.
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Generate Global Quality Agreements in accordance with templates and liaise with site and Suppliers to finalize to allow Supplier Quality Director approval. Catalent produces more than 70 billion doses per year, and each one will be used by someone who is counting on us.
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Adherence to BMS & OSHA Safety throughout all productions on-site and remote. Engage with BMS Films Senior Editor regularly to discuss and align on editing accomplishments, challenges and recommendations.
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Example: Weekend availability cannot fall on the same day; an associate must be available on two separate days (Friday and Saturday, Friday and Sunday or Saturday and Sunday). Organize stockroom by department and categories and stock merchandise on appropriate shelves or in offsite locations.
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Lead the project design and plan production for site development on a wide variety of projects, including site layout, grading, erosion and sediment control, site utilities, drainage, stormwater management, and associated civil engineering activities.
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