- Daiichi Sankyo, Inc. (Bernards, NJ)
- …as other research areas centered around rare diseases and immune disorders. SummaryThe Sr. Director , Data Quality and Integrity ( Global R&D & PV QA) ensures high ... solutions, integrates AI technologies, and drives process improvements. Collaborating with the Global QMS eCompliance team, the director oversees QA plans,… more
- Eisai, Inc (Nutley, NJ)
- …profile, we want to hear from you.The Associate Director supports the Eisai Global Oncology Business Unit for the Americas, EMEA, Japan, China, and Asia, by: ... Summary The Associate Director supports the Eisai Global Oncology Business Unit for the Americas,... Development Plan, Governance meeting deliverables. Support the development of Global sales and manufacturing forecasts… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …provide input and updates within internal cross-functional teams (eg, Diagnostic Development Teams) and to external diagnostic business partners specifically:Use ... Global Regulatory Strategy in the Drug and Device Development and Commercialization process.Experience with developing and documenting regulatory strategies in… more
- Repligen (Waltham, MA)
- OverviewThe Director , Global Payroll will lead the development and execution of Repligen's global payroll strategy tosupport a growing global ... the execution of Repligen's global payroll strategy. Design and implement global payroll policies, ensuring alignment with business goals and compliance… more
- Eisai, Inc (Nutley, NJ)
- …to ensure effective achievement of regulatory/ business objectives. The Executive Director will direct the development and submission of investigational drug ... want to hear from you. Job Summary The Executive Director , Regulatory Affairs will provide leadership and direction for... global regulatory leadership in support of the global development , registration, and life-cycle management of… more
- Eisai, Inc (Nutley, NJ)
- …project managers, line managers, clients and other stakeholders.Job Summary:The Associate Director , Global Alzheimer's Disease Project Management is responsible ... and oncology, with a strong emphasis on research and development . Our history includes the development of...for facilitating the operational aspects of the lecanemab global launch plan, provide project management, and serve as… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Module-related HRIS activities in the regions.Cooperate closely and trustfully with Global Business Process Owners and internal as external stakeholders, ... relevant area.ResponsibilitiesResponsible for the design, configuration, customizing and further development of the relevant SAP SuccessFactors modules with a...in particular with Global and Regional HRIT, HR Business , IT,… more
- Repligen (Waltham, MA)
- …mitigations to Senior Management across the organization, is essential.ResponsibilitiesThe Senior Director Global Regulatory Affairs must have the ability ... OverviewThe Senior Director , Global Regulatory Affairs will report...will monitor external product compliance requirement and advise the business on any changes and actions to be taken.… more
- Taiho Oncology (Bear, DE)
- Director , People Business Partner Europe Baar, Switzerland Req #460 Tuesday, May 20, 2025 Looking for a chance to make a meaningful difference in the oncology ... we earn and maintain the confidence of patients, the global healthcare community, collaborators and partners, and each other....us. Employee Value Proposition: Join Taiho Oncology Europe as Director People Business Partner Europe - Shape… more
- Merck & Co. (Lower Gwynedd, PA)
- Job DescriptionDirector - Early Development VaccinesDescriptionOur company is a global healthcare leader with a diversified portfolio of prescription medicines, ... 10 scientists to deliver bioanalytical solutions that enable and accelerate vaccine clinical development . The Director will report to the Executive Director … more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …other research areas centered around rare diseases and immune disorders. SummaryThe Executive Director , Head of Center of Excellence (CoE), Global Medical Safety ... for cardiovascular diseases, under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily… more
- Merck & Co. (North Wales, PA)
- …systems and processes for Individual Level of Influence Due Diligence.--Other Global Compliance Policies - Support development , maintenance, implementation, and ... Oversight team (the "Team") designs and helps implement our company's global compliance program, including compliance standards and processes (collectively, the… more
- Merck & Co. (Rahway, NJ)
- …final approval for all submissions and associated documentation. Provide expertise as the Global Regulatory Lead to Product Development Teams and the regulatory ... Job DescriptionThe Director / Principal Scientist, Regulatory Affairs Liaison , is...agencies for multiple indications simultaneouslyProvide expert advice as the Global Regulatory Lead to Product Development Teams… more
- Merck & Co. (Boston, MA)
- …- team in the role of Director . QP2-IO team is part of the Global Clinical Development organization and has oversight over drug development aspects ... development , with a strong, integrated understanding of the strategic elements of drug development . As a subject matter expert, the Director within the QP2-IO… more
- Eisai, Inc (Raleigh, NC)
- …, Western SCM Unit is also instrumental in supporting the various Business Development Due Diligence efforts and negotiations (in and out-licensing).The ... the launch of biologic products and hhceco initiatives, the Director will oversee Global Logistics and Import/Export...SCM Unit is also instrumental in supporting the various Business Development Due Diligence efforts and negotiations… more
- Merck & Co. (San Francisco, CA)
- …and Pharmacometrics (QP2) department drive model-informed drug discovery and development (MIDD) to routinely enable efficient drug discovery/ development ... at our Company, this position offers an opportunity for the Associate Director to drive pipeline impact across therapy areas.This Associate Director … more
- Merck & Co. (San Francisco, CA)
- …in the role of Associate Director QP2-IO team is part of the Global Clinical Development organization and has oversight over drug development aspects ... are emerging leaders in the field of quantitative drug development , with a developing understanding of the strategic elements...communication skills. As a subject matter expert, the Associate Director within the QP2-IO Group will work closely with… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …Novo Nordisk, you will have the opportunity to build a life-changing career in a global business environment. We encourage our employees to make the most of ... for leading company response from Deal to Contract (includes pre-deal assessment/analysis, development of business cases for Pricing Committee, offer … more
- Merck & Co. (Rahway, NJ)
- Job DescriptionAbout the Role:-As a Technical Lead, you will report into Director , Chemical Technical Operations, External Manufacturing API Technology, and play a ... External Partners. Foster proactive partnerships with External Partners to meet business goals, identify and mitigate risks, and continuously enhance performance.… more
- Merck & Co. (North Wales, PA)
- …a broad, comprehensive knowledge of statistics and its applications in clinical drug development . Primary Activities :Report to the Executive Director and Head ... a distinguished department within our company's renowned Research and Development division, quantitative scientists, in partnership with other subject matter… more
