- Merck & Co. (North Wales, PA)
- …knowledge of reporting processes (standard operating procedures) that align with regulatory requirements (eg, 21 CFR Part 11, ICH GCPs) and software development ... platforms, inspections, and related process and training for the global Statistical Programming organization.- The individual supports the organization to… more
- Merck & Co. (North Wales, PA)
- …of clinical development, including study design, initiation, execution, monitoring, analysis, regulatory reporting , publication, and presentation at national and ... or marketed vaccines that incorporate the latest scientific developments, regulatory requirements, the competitive landscape, and commercial considerationsPlanning clinical… more
- Rose International (Chicago, IL)
- …The Global Procurement team is seeking a Third-Party Management Reporting Specialist with extensive experience in SharePoint development, Nintex workflows, Power ... Only qualified Reporting Analyst candidates located near the Chicago, IL...as Power BI, Tableau, and Incorta, along with proven project management skills. They should excel in designing solutions… more
- DivIHN Integration Inc (Deerfield, IL)
- … and communication tools to ensure appropriate and timely communication and reporting from multiple projects and quality/ regulatory Core Team members Meeting ... Meghna at 224 369 4230 Sivanesan at 224 369 0756 Title: Senior Project Manager (HYBRID) Location: Deerfield, IL Duration: 6 Months (with possible extension) Hybrid… more
- Rose International (Jacksonville, FL)
- Only qualified Project Managers with extensive Workforce Management experience located near the Jacksonville, FL area will be considered due to the position ... for the future of the workforce. We are a global team with highly motivated colleagues who want to...a growth mindset, with a proactive can-do attitude to project delivery and "get things done" on a tight… more
- Merck & Co. (North Wales, PA)
- …art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for ... the benefit of patients and global human health. This position supports statistical programming activities for late stage drug/vaccine clinical development projects.… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …direction and securing execution of the following projects according to the Global Project Framework including the medical development strategies reflected in ... and future markets and business needs and leverage medical, scientific and regulatory opportunities. In agreement with the individual Project Vice President… more
- Merck & Co. (North Wales, PA)
- …art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for ... the benefit of patients and global human health. This position supports statistical programming activities for multiple and/or late stage drug/vaccine clinical… more
- Merck & Co. (Rahway, NJ)
- … reporting and interpretation of dataMaintain a comprehensive understanding of global regulatory expectations and shape, present and defend regulatory ... external vendors and partners, creating an aligned, quantitative and model-informed regulatory framework to impact strategies and decisions of drug discovery and… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Is safety representative in cross functional project teams as needed eg Global Project Team (GPT) Plan, execute and drive all activities related to ... safety surveillance sub-function within the US East Coast Development Hub comprised of Senior Global Safety Leads, Global Safety Leads and Senior Global … more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …units to ensure unified Global Clinical Science Strategy. In conjunction with Global RD Finance, Global Project Management, HR, manage the workforce ... be the Clinical Science Group Lead in late phase development in the Global Clinical Science function. He/she will be responsible for managing the multiple Clinical… more
- Merck & Co. (Washington, DC)
- …Executive Director, Policy Development, Strategy, and Capabilities, the AVP, and VP Global Public Policy. Reporting to the Executive Director, Policy Development ... public policy issues and geo-political changes that will impact our global business.The Director independently and proactively identifies risks and opportunities,… more
- Merck & Co. (Rahway, NJ)
- …Director, Policy Development and Strategy is a key leadership role in the Global Public Policy Strategic Planning & External Engagement team, with responsibility for ... risk and leverage opportunities in support of our company's business priorities. Reporting to the Associate Vice President, Strategic Planning & External Engagement,… 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)
- …CMR, Global , Field Sales, Account Management, Analytics, Investor Relations, Regulatory , and all others, including global colleagues/counterparts, on a ... CMR, HEOR, Global , Field Sales, Account Management, Analytics, Investor Relations, Regulatory , and all others on a routine basis Liaises with HQ counterparts on… more
- Merck & Co. (Washington, DC)
- …policy development across the Strategic Planning & External Engagement team, reporting to the Executive Director, Policy Development & Strategy.The Associate ... with the Executive Director to ensure that they are fit for purpose for global , regional, and country policy planning and activity tracking. The role will also… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …for cardiovascular diseases, under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily ... roadmap, leading innovation, communication strategies, identifying and managing KPI's, reporting strategies, and the implementation of system enhancements in areas… more
- Novo Nordisk Inc. (WA)
- 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. (North Wales, PA)
- …company's process es and standards to ensure compliance with internal policy, regulatory requirements, and health literacy principles . - Under the supervision of ... with internal and external reviewers to ensure it meets regulatory requirements while leading the summary through review and...language structured content and graphic libraries - Ensu ring Project Leads and management are informed of problems or… more
- Novo Nordisk Inc. (Irvine, CA)
- 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
