- Tris Pharma (Monmouth Junction, NJ)
- …in our Monmouth Junction, NJ facility for an experienced MD to serve as Senior Director or Director , Clinical Development. Title and salary commensurate ... clinical study conduct; Collaborates closely with internal stakeholders, (ie Regulatory Affairs, Product Development, Research and Development (R&D), Quality… more
- Eisai, Inc (Nutley, NJ)
- …a difference. If this is your profile, we want to hear from you.The Sr Medical Director provides medical leadership for medical affairs strategy, planning and ... and scientific communication/publication components of overall medical operating plan.The Sr Medical Director provides strategic development, planning,… more
- Insmed Incorporated (Bridgewater, NJ)
- …New York™, and Best Workplaces for Millennials™ lists.OverviewReporting to the Executive Director Quality GMP Compliance, the Director , Quality Operations will ... related issues. Impact assessment includes proper evaluation for Health Authority reporting (FAR, Quality Defect, Recalls, etc) and escalation within QA.Responsible… more
- Eisai, Inc (Nutley, NJ)
- …Associate Director , Omnichannel Marketing and Media position reports to the Senior Director , Omnichannel Marketing (HCP and Patient). The associate ... deliver omnichannel and media specific marketing input and activities.The Associate Director of Omnichannel Marketing and Media is responsible for managing,… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …other research areas centered around rare diseases and immune disorders.Summary The Senior Director sits within Global Oncology Clinical Development, an ... the Target Product Profile (TPP)- Development of clinical sections of trial-level regulatory documents (eg, response to HAs, briefing book, etc.) in conjunction with… more
- Insmed Incorporated (Bridgewater, NJ)
- … Director , Toxicology, is a key member of the nonclinical safety team, reporting to the Executive Director , Head of Toxicology and Molecular Mechanisms. In ... DABT/DACVP certification preferred. Minimum of 15 years of experience as a regulatory toxicologist (study director /monitor and/or project lead) in the… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …quality standards and timelines and that quality of data is suitable for regulatory submission. The Associate Director will have routine interaction with key ... clinical study plan and execution (from planning start-up, conduct, reporting and close out) including timeline, quality and budget....and share with study team, Operations Program Lead, and Sr . Director for the compound, on regular… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …this role, the incumbent will help develop multiple products. In doing so, the Senior Medical Director will work across different functional teams to support the ... Are you ready to make a difference?The Position We are seeking an enthusiastic Senior Medical Doctor with a high degree of scientific acumen who is excited by… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …ideally including time in role such as a Global Project Leader at Sr . Director level or equivalent preferred- Relevant therapeutic experience and proven ... areas centered around rare diseases and immune disorders.Summary The Executive Director , Global Clinical Operations Study Management Group Head has leadership and… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …global project teams. This role will be a senior member of the Regulatory , Quality and Clinical Reporting (RQC) team, and will provide mentorship and ... the written deliverables that support the clinical development and regulatory requirements of a clinical program. The Director...Writing team. Relationships The Director Medical Writing ( Director ) reports to a Senior Director… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …responsible for managing the multiple Clinical Science Asset Leaders (CSALs) at the Senior Director level for each respective programThis Clinical Science (CS) ... lead will also contribute to the program study strategy, planning, execution, and reporting outputs in collaboration with the CS Asset LeadsThe CS Group Lead will… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …operational and project management capabilities are essential for success. Relationships Reporting to the Director of Medical Omnichannel Engagement (MOE). ... About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one...ready to make a difference? The Position The Associate Director , Medical Affairs Omnichannel Engagement, role is to support… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …the treatment of multiple myeloma. Legend Biotech is seeking an Associate Director for Operations Compliance and Investigations Managementas part of the Technical ... Operations team based in Raritan, NJ. Role Overview The Associate Director for Operations Compliance and Investigations Management will provide strategic direction… more
- Daiichi Sankyo, Inc. (Basking Ridge, NJ)
- …and related materials that pertain to training objectives for use at Senior Leadership meetings.Special Projects/Change ManagementAssist the Director in the ... be part of the Compliance organization and will report directly to the Director , Compliance Training, Policy & Communications. This position will be responsible for… more
- 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 ... organization. From health-care-provider interactions and developing and implementing regulatory strategies with the FDA to providing medical education and collecting… more
- Citigroup (Queens, NY)
- The Senior Group Manager position is an integral member of the Global Regulatory Reporting Group (GRR). The GRR Group is a high-profile function, providing ... FR Y-15. + Provide oversight and thought leadership across Regulatory Reporting governance and activities across Citigroup,...with financial analysis in order to communicate results to Senior Management and US Regulatory Agencies. +… more
- Citigroup (New York, NY)
- The Regulatory Risk Sr Officer II is...company. + Professional ability and presence to interact with Senior Bank, Regulatory and Audit Management. + ... skills required in order to negotiate internally, often at a senior level. Some external communication is typically required. Provides advanced judgment… more
- Citigroup (Queens, NY)
- …impacting the FR Y-14 reporting . This role is part of the Global Regulatory Reporting Controllers function that has oversight and ownership of the FR Y-14 ... The Finance FR Y-14 Actuals Reporting Group Manager is a senior ...Country/Product Controllers, Technology, Finance, Risk and counterparts in Global Regulatory Reporting . **Responsibilities:** + Produces materially complete… more
- J&J Family of Companies (Raritan, NJ)
- …of the Johnson & Johnson Family of Companies, is recruiting for a Director / Senior Director , Clinical Rseearch Physician for **Late Development Oncology** ... Medical Director / Sr . Medical Director ,...with other functional disciplines, including GCO, Data Management, Statistics, Regulatory , QMMC, and GMS to ensure flawless and integrated… more
- Teva Pharmaceuticals (Parsippany, NJ)
- Sr Director , Global Launch Readiness - Immunology Date: May 25, 2024 Location: Parsippany, United States, New Jersey, 07054 Company: Teva Pharmaceuticals Job Id: ... messaging, positioning, creative campaign development and regional alignment/coordination). The Senior Director , Global Launch Readiness Immunology will be… more
