- 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
- Merck & Co. (Rahway, NJ)
- …clinical development, including study design, placement, monitoring, analysis, regulatory reporting , and publication. - Specifically, the Senior Director may ... and dedicated colleagues while developing and expanding your career. - The Senior Director ( Senior Principal Scientist) has primary responsibility for the… more
- Merck & Co. (Rahway, NJ)
- …cycle of clinical development, including study design, placement, monitoring, analysis, regulatory reporting , and publication.Specifically, The Senior ... talented and dedicated colleagues while developing and expanding your career.The Senior Director (Sr. Principal Scientist) has primary responsibility for the… 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
- Novo Nordisk Inc. (Plainsboro, NJ)
- …internal stakeholders include Medical & Science, Clinical Operations, Regulatory Affairs, Data Management, Biostatistics, Non-clinical, Medical Affairs, Marketing, ... ine management responsibility of Director/Associate Director Global Safety Lead, Senior Global Safety Scientist(s)/Global Safety Scientist(s) within the Safety… more
- Merck & Co. (North Wales, PA)
- …figures), which range from individual clinical trials to worldwide regulatory application submissions and post marketing support.Design and maintain statistical ... SAS programming in a clinical trial environment; developing analysis and reporting deliverables for Research and Development projects (data, analyses, tables,… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …you in? Are you ready to experiment with us? The Position The HCP Senior Strategist will be a pivotal driver in shaping an insights-driven HCP marketing strategy ... affairs, market access and policy/advocacy (MAPA), Centres of Excellence (COEs), regulatory affairs, other relevant NNI departments, and external stakeholders to… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …monthly status reports on closing process to the Associate Director of Accounting, the Senior Director of Accounting and the VP of Finance and Supply Chain Guide the ... Senior Accountant and Global Shared Service team of 3-4...with the current and new GAAP or International Financial Reporting Standards (IFRS). Coordinates US response and recommendation for… more
- Legend Biotech USA, Inc. (Iowa City, IA)
- …in accordance with Corporate, PhRMA, and OIG guidelinesStrict compliance with all regulatory agencies, state , and federal law is requiredAdheres to company ... of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking Senior Cell Therapy Account Specialist as part of the Commercial team based Remote… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …training on new procedures, to auditing against local and corporate policies, to reporting compliance-related issues, ECP keeps us accountable every step of the way ... A minimum of eight (8) years combined pharmaceutical, legal, regulatory , and compliance experience required OR a minimum of...veteran status or any other characteristic protected by local, state or federal laws, rules or regulations. If you… more
- Merck & Co. (South San Francisco, CA)
- …provide scientific and technical leadershipEnsure high-quality data generation, analysis, and reporting to project teams, governance bodies, and regulatory ... your rights, including under California, Colorado and other US State Acts US Hybrid Work Model Effective September 5,...in a manner consistent with the requirements of applicable state and local laws, including the City of Los… 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
- Novo Nordisk Inc. (Plainsboro, NJ)
- …lives for a living. Are you ready to make a difference? The Position Reporting to the head of Clinical, medical, Regulatory (CMR) Business Operations, the ... of Regulatory and Compliance requirements related to Pharmaceutical Pharmacovigilance/Safety reporting Advanced capability in MS Excel, MS PowerPoint and MS Word… more
- Merck & Co. (Rahway, NJ)
- …including development strategy, study design, initiation, execution, monitoring, analysis, regulatory reporting , publication, and presentation at national and ... teams manage studies to provide the safety and efficacy data required for regulatory approval of potential new drugs and new indications for existing products. We… 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
- Novo Nordisk Inc. (Plainsboro, NJ)
- …for reporting , training internal stakeholders, and staying updated with regulatory changes Physical Requirements Hybrid Policy: 3 days in office, 2 days ... Area leads, Sales, Patient Support Program, CIA&A, Medical, Legal, and Regulatory and IT. Essential Functions Portal Strategy Development: Leading the development… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …and customer groups. The owner is responsible for coordinating with agencies for regulatory review planning, and ensuring best practices in SEO and SEM. The owner ... and Omnichannel Orchestration teams on coordination with agencies for Medical/ Regulatory /Legal review planning schedules Best Practice Research and Documentation:… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …members, Global commercial and New Product Planning teams, Medical Affairs, Regulatory Affairs, Legal, and Market Access. Collaborates closely with Enterprise ... Leads development of a strategic insights plans in conjunction with Senior Director Enterprise Intelligence and incorporate market research and analytics needs… more
- Merck & Co. (Durham, NC)
- Job DescriptionPosition Description: Senior Specialist, Quality Assurance Our Company will construct a new manufacturing facility to significantly expand its ... growth, harvest, lyophilization, product inspection, and quality control laboratories.The Senior Quality Assurance Specialist will support this expansion. Project… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …affairs, market access and policy/advocacy (MAPA), Centers of Excellence (COEs), regulatory affairs, and other relevant NNI departments to ensure alignment of ... providing regular updates to leadership Product Evolution: Oversee product strategy and regulatory activities related to new clinical data or label changes. Lead… more
