- Daiichi Sankyo, Inc. (Bernards, NJ)
- …governance processes, and on Joint Alliances.Assess and articulate regional interdependencies, program regulatory risks, and opportunities in the development of ... project meetings.Provide guidance to peers and cross-functional team members regarding strategic regulatory issues.Develop timeline and strategic input… more
- Merck & Co. (Rahway, NJ)
- …of regulatory environment, and vision to influence the regulatory environmentWill be responsible for sub-functional strategic planning, coordinating, ... oral and non-oral portfolio. Within Biologics and Biopharmaceutics, the Biopharmaceutics Director will influence the strategy, lead activities, and develop a team… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders. Summary: The Associate Director will lead the execution and lifecycle management of Global Medical Affairs' ... both IIS and collaborative studies. Ensure projects align with strategic goals and compliance standards from initiation through completion.Operational Strategy:… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …for managing the multiple Clinical Science Asset Leaders (CSALs) at the Senior Director level for each respective program . This Clinical Science (CS) Group ... Lead will be responsible for overseeing multiple program -level CS Asset Leads who are managing a team...RD leaders in Clinical Operations, Biostatistics and Data Management, Regulatory Affairs, and other RD functions to ensure effective… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders.Summary: The Associate Director , Regional Marketing Conventions & Field Programs will be responsible for ... more, while ensuring adherence to DS policies and procedures. The Associate Director , Regional Marketing Conventions & Field Programs is responsible for managing the… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Such trials could be pivotal for submission; Prepares clinical section of regulatory documents; Oversees management and performance of CRO; Participates in creation ... of developmental and regulatory strategy; Drafts protocol profiles and sections of key...For large or complex Phase 2 studies: Provides the strategic direction to BD&O for EDC, edit checks, data… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Such trials could be pivotal for submission; Prepares clinical section of regulatory documents; Oversees management and performance of CRO; Participates in creation ... of developmental and regulatory strategy; Drafts protocol profiles and sections of key...For large or complex Phase 2 studies: Provides the strategic direction to BD&O for EDC, edit checks, data… more
- Merck & Co. (Rahway, NJ)
- …of regulatory environment, and vision to influence the regulatory environmentWill be responsible for sub-functional strategic planning, coordinating, ... portfolio. Within Biologics and Biopharmaceutics, the large molecule product development Director will influence the strategy, lead activities, and develop a team… more
- Tris Pharma (Monmouth Junction, NJ)
- …from you.We are hiring at our Monmouth Junction NJ Headquarters for a Senior Director to lead our small, but productive, Marketing team.The Senior Director , Head ... development and execution of brand marketing strategiesLeads and participates in strategic and operational creation and implementation of annual strategic … more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …complexity in design and geographic scope). Prepares clinical section of regulatory document. Collaborates as team member with AROs/CROs. Drafts development plans, ... Represents Clinical Development on Project Teams. ResponsibilitiesStudy Strategy: Provides the strategic direction to Biostats Data Mgmt & Data Ops for EDC,… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …head). They will coordinate with other TA functions including Medical Directors, Alignment Director , Program Development Director and the Medical Liaison ... About the Department The Clinical, Medical and Regulatory (CMR) department at Novo Nordisk is one...ready to make a difference? The Position The Scientific Director (SD) functions as a subject matter expert to… more
- Merck & Co. (Rahway, NJ)
- …to bring analytical representation and expertise to project teams and support regulatory filings (eg, INDs/IMPDs and BLAs).-The Director selects, trains, and ... Job DescriptionThe Director of Biologics Potency in Analytical Research &...in Analytical Research & Development is responsible for providing strategic and technical leadership for a portion of the… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …needs and KPIs Develop a comprehensive marketing strategy, plan, and program architecture, supporting each partnership's business priorities, with the goal of ... partnership and driving value for stakeholders Supplier relationships: Drives Strategic Sourcing for Therapeutic Areas and Commercial needs: Identify, evaluate,… more
- Merck & Co. (Rahway, NJ)
- …in support of our company's lung, head & neck, and melanoma oncology program ; heavy emphasis on milestone communications ( regulatory approvals, data releases, ... Job DescriptionThe role of Director , Global Communications, Oncology is a unique opportunity...with Global & US Oncology marketing leaders to develop strategic communications aligned with key business priorities.Proactively evaluate innovative… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …to jointly develop and commercialize ciltacabtagene autolecuel (cilta-cel) in 2017. Our strategic partnership is designed to combine the strengths and expertise of ... in the treatment of multiple myeloma.Legend Biotech is seeking Global Commercial Program Head as part of the Technical Operations team based in Raritan,… more
- Legend Biotech USA, Inc. (Piscataway, NJ)
- …to jointly develop and commercialize ciltacabtagene autolecuel (cilta-cel) in 2017. Our strategic partnership is designed to combine the strengths and expertise of ... in the treatment of multiple myeloma.Legend Biotech is seeking an Associate Director Immuno-Oncology as part of the Research and Development team based in… more
- Insmed Incorporated (San Diego, CA)
- …for Millennials™, and Best Medium Workplaces™ lists.OverviewThe Executive Medical Director of Ophthalmology, Clinical Development holds the responsibility to lead ... & interpretation of clinical trial data, authoring clinical study and regulatory communications and documents, and monitoring of competitor activities and data.… more
- Legend Biotech USA, Inc. (Raritan, NJ)
- …to jointly develop and commercialize ciltacabtagene autolecuel (cilta-cel) in 2017. Our strategic partnership is designed to combine the strengths and expertise of ... of an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking Director , Global Process Validation as part of the Technical Operations team based… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …CS&M, CMR, Global, Field Sales, Account Management, Analytics, Investor Relations, Regulatory , and all others, including global colleagues/counterparts, on a routine ... the franchise, and is accountable for meeting business objectives Ensures strategic alignment between the Value Communication and Contracting Strategy, and between… more
- Merck & Co. (North Wales, PA)
- …development, including study design, initiation, execution, monitoring, analysis, regulatory reporting, publication, and presentation at national and international ... or marketed vaccines that incorporate the latest scientific developments, regulatory requirements, the competitive landscape, and commercial considerationsPlanning clinical… more
