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The Executive Director, Global Cell Therapy Organization (CTO), Strategy & Operations (S&O) will act as a key partner to the Cell Therapy Strategy & Operations Vice President and Cell Therapy Leadership Team (CTLT.
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The Executive Director will report to the Vice President, CT Strategy and Operations. Lead team of six (one Senior Director, three Directors, one Associate Director and one Senior Manager) to develop vision, strategies and plans to build performance-centric systems, tools and communication tools to achieve CTO objectives.
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The Executive Director also serves on the University Services Emergency Operations group, working closely with the offices of Public Safety and Environment Health and Safety to plan for and respond to emergency situations.
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The Associate Director of Marketing is a team leader recognized for their ability to influence matrix team members and manage multiple agencies for the successful development and execution of both HCP and patient promotion plans.
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Supports the Director of Nursing (Resident Services Director) in the administration of the nursing services. The Resident Service Designee in concert with the Director of Nursing assumes responsibility for providing oversight of the resident health care service’s needs, including the overall medication delivery system and the coordination of in-service training for the Resident Care Services Department.
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Johnson & Johnson Innovative Medicine is currently seeking an Associate Director, Neuroscience Digital Health – Neurodegeneration to be located at one of our sites in Cambridge, MA, Titusville, NJ, or La Jolla, CA.
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This role is responsible for driving Commercial Operations for an EVERSANA™ COMPLETE Commercialization program by coordinating with our business units/functional areas who enable our marketing, medical and field teams, to drive operational excellence.
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As an Associate Director, Biostatistician, you will be a champion of Otsuka's culture and values and will be responsible for providing statistical expertise/input in the drug development, including clinical development plan and regulatory submission strategy.
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The Director Information Security will report directly to the VP and Global Head of Information Security and IT Risk & Compliance, playing a strategic role in the Information Security Leadership Team.
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As the Program Director, you will work within our certified community behavioral health clinic (CCBHC) in Trenton, Mercer County NJ. The CCBHC program features a new approach to care designed to improve overall health by treating the whole person through community based mental health and addiction treatment, with a focus on helping link clients to physical health, community-based and employment/educational resources.
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Job title: Music Director. An undergraduate degree in music with a vocal/keyboard/piano/guitar proficiency in protestant music and able to direct and accompany a praise and worship team OR a minimum of five years' experience in leading a praise and worship team on vocal keyboard/piano/guitar in protestant music.
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Run franchise operations to ensure revenue and profitability targets are met. Oversee employee training in areas such as sales, logistics, operations, marketing, customer service, profitability, and safety.
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The Role: Director of Data Science – NLP, LLM and GenAI. The Team: S&P is a leader in risk management solutions leveraging automation and AI/ML. This role is a unique opportunity for an experienced ML scientist and hands-on NLP/Gen AI/ LLM senior scientist to grow into the next step in their career journey and apply her or his domain expertise in NLP, deep learning, GenAI, and LLMs to drive business value for multiple stakeholders while mentoring and growing a ML Data Science team.
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This position reports to Head of Biostatistics and Data Management (BDM) within Research and Development (R&D) Department at SPARC. Main responsibilities will include effective leadership, planning and oversight within the Clinical Data Management (CDM) function as well as facilitating collaboration across all R&D functions to ensure rigorous collection and analysis of data.
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Provides oversight on scientific management of preclinical safety assessment/toxicology studies supporting early drug development spanning lead optimization through IND and NDA submissions and nonclinical post-marketing approval requirements.
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