- Eisai, Inc (Nutley, NJ)
- …industry preferred.Skills:Eisai Salary Transparency Language:The base salary range for the Executive Director , Global Regulatory Affairs - Neurology is from ... Affairs will provide leadership and direction for the global regulatory aspects of Eisai's products under...the employment eligibility of all new hires in the United States . Please click on the following… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …partner side) CDx RA Policy and Intelligence : Keep abreast of the changing global regulatory environment for devices and share/educate CDx department on these ... procedures.Understanding of strategic and tactical role and deliverables of Global Regulatory Strategy in the Drug and...to 10% Occasional travel to Health Authority meetings in US and Europe, potentially Japan Daiichi Sankyo, Inc. is… more
- Merck & Co. (Rahway, NJ)
- Job Description Director , Combination Product Regulatory CMC - (R5)- - - This Principal Scientist position is equivalent to a Director position. Under ... CMC Team Leader, the Principal Scientist is responsible for executing in the Regulatory CMC space. - Leveraging demonstrated capability in Regulatory CMC, this… more
- Eisai, Inc (Nutley, NJ)
- …employers to electronically verify the employment eligibility of all new hires in the United States . Please click on the following link for more information: ... profile, we want to hear from you. The Associate Director (AD), Global Medical Affairs Training and...Advisory Board Reports, and strategic Insights Reports to Eisai US and Global Medical Affairs organization.Strengthen Medical… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThis position will be part of the Device Quality & Regulatory Team within Global Regulatory Affairs and Clinical Safety (GRACS). The primary ... medical device combination quality system aspects are integratedStay abreast of evolving global regulatory landscapes for medical device and medical device… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking a Director , Global Sourcing (Direct Materials) as part of the Technical ... Operations team based in Raritan, NJ.Role OverviewThe Director , Global Sourcing (Direct Materials) is responsible for leading the design and execution of a… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Director , Global Scientific and Value Content-Healthcare Professional (Dir GSVC-HCP) for oncology is a headquarters-based leadership role ... within Global Medical and Value Capabilities (GMVC) organization. The role...GSVC plans for one or more products and disease states , ensuring alignment with the GMSA V&I Plans.Incorporating Medical… more
- Merck & Co. (Durham, NC)
- …Maintenance, Safety, Process Development, Technical Services, Utilities and Validation.-- Director Global Engineering Services Construction and Logistics ... performing group of technical professionals.An understanding of GMP and regulatory qualification requirements and expectations are desirable.-Pharmaceutical industry experienceConstruction… more
- Merck & Co. (Rahway, NJ)
- …and project delivery.A complete understanding of ICH GCP and Global /Regional/Local regulatory requirements is required.Strong Communication skills requiring ... Job DescriptionThe Executive Director (ED) is the Clinical Operations lead in...scope for GCTO country operations.Adherence to GCP, local and global policies and procedures to conduct high-quality, inspection ready… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Leads US FDA/EU EMA interactions with support from higher-level manager. Regulatory Knowledge: Demonstrates expert knowledge of US /EU regulatory ... 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… more
- Eisai, Inc (Nutley, NJ)
- …employers to electronically verify the employment eligibility of all new hires in the United States . Please click on the following link for more information: ... profile, we want to hear from you. The Executive Director , Global Clinical Development resides within the...with external key opinion leaders, advisors as well as US and EU regulatory bodies in order… more
- Eisai, Inc (Nutley, NJ)
- …employers to electronically verify the employment eligibility of all new hires in the United States . Please click on the following link for more information: ... difference. If this is your profile, we want to hear from you. Director , HCP Marketing, Alzheimer's Disease will lead several core marketing, strategy, and lifecycle… more
- Merck & Co. (Rahway, NJ)
- …Divisional and Regional Quality/Management councilsProvide guidance and consultation services for regulatory reporting (eg, BPDR, DPR)Author and/or review global ... Job DescriptionThe Quality Assurance Director will provide compliance leadership and direction to...implementation and effectiveness to ensure no recurrence of findingsGather regulatory intelligence and partner with our Company and CMO… more
- Genmab (NJ)
- …you and feel like a fit? Then we would love to have you join us !The RoleThe Associate Director acts as a statistical expert supporting the clinical development ... and serious diseases. We strive to create, champion and maintain a global workplace where individuals' unique contributions are valued and drive innovative solutions… more
- Eisai, Inc (Nutley, NJ)
- …employers to electronically verify the employment eligibility of all new hires in the United States . Please click on the following link for more information: ... your profile, we want to hear from you. Associate Director , Medical Education - Oncology, is responsible for the...focus of these plans and activities will be either global , US -focused with intended use and adaptation… more
- Merck & Co. (Rahway, NJ)
- …execution, reporting and interpretation of data. Maintain a comprehensive understanding of global regulatory expectations and shape, present and defend ... Point, PA / Rahway, NJ is seeking a curious and collaborative Associate Director to support our rapidly expanding cardiometabolic and ophthalmology pipelines. - As… more
- Merck & Co. (Rahway, NJ)
- …optimizing model-based analyses on programs Maintaining a comprehensive understanding of global regulatory expectations for small molecules and biologics ... - Immune/Oncology (QP2-IO) team in the role of Associate Director , Quantitative Systems Pharmacology (QSP) . QP2-IO team is...communication. Experience in IND, BLA and other submissions to global regulatory agencies. An exemplary record of… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …value through human-centered design pull you in? Are you ready to experiment with us ? The Position The Associate Director of Nephrology Key Opinion Leader ... team culture that is made up of diverse skillsets, united by the shared belief that reinvention and learning...endorsement, ensuring executable strategies are in place. Advocate for US marketing initiatives within the context of global… more
- Merck & Co. (North Wales, PA)
- …optimizing model-based analyses on programs. Maintaining a comprehensive understanding of global regulatory expectations for small molecules and biologics ... and verbal communication. Experience in IND, NDA and other submissions to global regulatory agencies. An exemplary record of increasing responsibility,… more
- Merck & Co. (Rahway, NJ)
- …Small Molecule Analytical Research and Development (SMAR&D) team has an opening for a Director based in Rahway, NJ. Join us and experience our culture first-hand ... technologies and predictive analytical tools. As part of our global team, you will have the opportunity to collaborate...for always maintaining a state of inspection readiness.- The Director should be well engaged with regulatory … more
