- Genmab (Plainsboro, NJ)
- …to be our best, and authentic is essential to fulfilling our purpose.The RoleThe Global Regulatory Labeling Strategy Sr Manager /Associate Director will be ... information) for the Genmab portfolio of products. This role will be within Global Regulatory Affairs (GRA) and will report to the Sr Director, Labeling, Policy… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …US regulatory activities. The Manager RPM is responsible for supporting the global regulatory lead (GRL), US regulatory lead (USRL) and global ... as other research areas centered around rare diseases and immune disorders.Summary The Manager , Regulatory Affairs - Regulatory Project Management (RPM)… more
- Eclaro (Charlotte, NC)
- Audit Manager , Global Markets Operations (GMO) and Non-Financial Regulatory Reporting, Tax & Credit Job Number: 24-03089 Grab the opportunity to achieve your ... full potential! ECLARO is looking for an Audit Manager , Global Markets Operations (GMO) and Non-Financial Regulatory Reporting, Tax & Credit for our client… more
- Merck & Co. (North Wales, PA)
- …Affairs Headquarters Principal Scientist is responsible for development and implementation of global regulatory strategy for their assigned projects in the ... regulatory oversight for assigned products, functioning as the single, accountable, global regulatory point of contact on those projects within Global… more
- Eisai, Inc (Raleigh, NC)
- …a difference. If this is your profile, we want to hear from you.The Project Manager , Global Supply Chain is responsible for supply related projects and global ... and Operations to effectively challenge project deliverables and milestones.The Project Manager , Global Supply Chain will develop robust communication processes… 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
- Eisai, Inc (Nutley, NJ)
- …to the Executive Director, IT Security, Compliance, & Architecture, s/he is the Global IT department's trusted leader and manager who assesses and provides ... difference. If this is your profile, we want to hear from you.The Director, Global IT Governance, Risk & Controls Management Lead is responsible for overseeing the… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …GxP and Non-GxP activities, assuring that these systems are compliant with global regulatory and Daiichi Sankyo requirements, and business expectations. Executes ... a risk-based framework (Computer Software Assurance (CSA)) that is compliant with global regulatory expectations and business expectations to execute … more
- Merck & Co. (Durham, NC)
- Job Description GENERAL SUMMARY :Our company is expanding its global Bacillus Calmette Guerin (BCG)_vaccine production by adding an end-to-end manufacturing and ... finished product, and laboratory testing for the BCG vaccine.The Quality Operations Laboratory Manager leads a team of analysts in the start-up and method transfer… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …business management team, as well as the broader North America Clinical, Medical and Regulatory (CMR) function and global stakeholders in Global Development ... About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one...trial strategy and execution to targets. Co-leads communication to global and local stakeholders to ensure consistency. Proactively identifies… 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 ... research areas centered around rare diseases and immune disorders. Summary The Manager , Clinical Data Standards is responsible for the development and sustainability… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …medicines to help people. Under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily ... research areas centered around rare diseases and immune disorders. Summary The Manager External Data Management, is accountable for an end-to-end delivery of… 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
- Legend Biotech USA, Inc. (Raritan, NJ)
- Company InformationLegend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. Headquartered in Somerset, ... and natural killer (NK) cell-based immunotherapy.Legend Biotech entered into a global collaboration agreement with Janssen, one of the pharmaceutical companies of… 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 ... around rare diseases and immune disorders. Job Summary: The position of Manager Scientific Operation, Precision Medicine (PrM) will be responsible for managing a… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …pharmaceutical industry Minimum 2 years of experience as a Clinical Trial/Project Manager Experience with global clinical trial operations, in multiple phases ... About the Department Our East Coast Global Development Hub brings together the best minds...Position We are looking to hire a Clinical Project Manager (CPM). This is a unique opportunity to work… more
- Aequor (Golden Valley, MN)
- …This is a hybrid role Full-Time We are seeking an experienced and motivated Project Manager to lead the refresh and update of our Supplier Code of Conduct. This role ... of Conduct to identify areas for improvement. Research industry standards and regulatory requirements to ensure the updated Code meets or exceeds current… more
- Aequor (Thousand Oaks, CA)
- …on time. The qualified candidate will support verification, validation, and regulatory submissions of these devices. Work within a cross-functional organization to ... functions.Responsibilities:Lead medium/small projects independently and work directly with Program Manager on large multi-year programs. Managing the overall program… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- Company InformationLegend Biotech is a global biotechnology company dedicated to treating, and one day curing, life-threatening diseases. Headquartered in Somerset, ... and natural killer (NK) cell-based immunotherapy.Legend Biotech entered into a global collaboration agreement with Janssen, one of the pharmaceutical companies of… more
- Genmab (Plainsboro, NJ)
- …purpose.The Role & Department As a Senior Programming Associate or Programming Manager , you will be in the Statistical Programming team and Development Operations ... the programming department.Contributes to ongoing improvements in cross-functional and global collaboration and sharing of better practices and knowledge.Maintains… more
Related Job Searches:
Global,
Global Manager,
Global Program Regulatory Manager,
Global Regulatory Policy Manager,
Manager,
Manager Global Regulatory Affairs,
Regulatory,
Regulatory Manager,
Senior Manager Global Regulatory,
Sr Manager Global Regulatory