- Merck & Co. (Rahway, NJ)
- …to improve and save lives of women with breast and gynecological cancers. Associate Director Global Oncology Marketing Women's Cancer Portfolio Key ... working and governance teams (launch readiness reviews, identification of data gaps and approaches, organized customer interactions, market research, demand,… more
- Merck & Co. (Rahway, NJ)
- …oral and non-oral portfolio. Within Biologics and Biopharmaceutics, the Biopharmaceutics Director will influence the strategy, lead activities, and develop a team ... portfolio and influence bridging strategies across the portfolio. The Biopharmaceutics Director will work with their direct reports to proactively develop and… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionWe are seeking a dynamic and visionary leader for the role of Associate Director , Community Exchange Manager. This person will be responsible for ... building strong community relations related to digital, data , and analytics within HHDDA and across the Human Health organization. They will also drive cultural… more
- Merck & Co. (Rahway, NJ)
- …Global Template asset, delivering enterprise-level capabilities through harmonized business processes and data .- The team is responsible for the operation of all our ... Company SAP and integrated solutions, governance of the associated enterprise assets, and cost-effective delivery of capabilities to support achievement of immediate and future state business objectives. Within the EIT SAP Platform Team, the EIT SAP Basis… more
- Merck & Co. (Rahway, NJ)
- …digital, data and analytics and measuring the impact.The Executive Director , Head of Oncology Global Commercial Pipeline Analytics, HHDDA will be responsible ... data science, payer insights & analytics, and data strategy & solutions).Reporting to the Associate ...and data strategy & solutions).Reporting to the Associate Vice President of Global Commercial Pipeline analytics within… more
- Merck & Co. (Rahway, NJ)
- …the Quantitative Pharmacology and Pharmacometrics - Immune/Oncology team in the role of Associate Director . The team is part of the Global Clinical Development ... of drug development and effective communication skills. As a subject matter expert, the Associate Director within the Group will work closely with teams of… more
- Merck & Co. (Rahway, NJ)
- …portfolio. Within Biologics and Biopharmaceutics, the large molecule product development Director will influence the strategy, lead activities, and develop a team ... compliance mindset and collaboration with various partners and stakeholders in development.The Director will report to the Executive Director of Biologics and… more
- Merck & Co. (Rahway, NJ)
- …those described in the Pipeline Advertisement.As a strategic marketing position, the Associate Director will provide recommendations that will contribute to ... media to evaluate recommendations that align with the target audience.- Analyzing data , media measurement, and analytics to ensure ongoing optimization and success… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Director of Biologics Potency in Analytical Research & Development is responsible for providing strategic and technical leadership for a portion ... partnering to build a culture of innovation and inclusion.-The Director reports to the Executive Director , Cell...responsible for a team of approximately 10-15 senior and associate level scientists in Rahway, New Jersey. -The position… more
- Legend Biotech USA, Inc. (Piscataway, NJ)
- …an immunotherapy in the treatment of multiple myeloma.Legend Biotech is seeking an Associate Director Immuno-Oncology as part of the Research and Development ... cell-based therapies. We are seeking an experienced and dynamic Associate Director to lead our in vivo...execute experiments, document, and interpret scientific results, present the data to cross-functional teamsIn vivo study design and assay… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …other research areas centered around rare diseases and immune disorders. Job Summary: The Associate Director of Regulatory Writing is a key role responsible for ... and strategic insights at the study team level. The Associate Director of Regulatory Writing must possess...study team level including recommendations for and review of data outputs for collection of specific data … more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …as other research areas centered around rare diseases and immune disorders.Summary The Associate Director of ERP Applications is responsible for overseeing and ... areas/ SAP Finance modules: Asset Management, General Ledger, Travel Management, Master Data , Procure to Pay, Invoice to Pay, Project Systems, Taxes, Vertex… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …other research areas centered around rare diseases and immune disorders.Summary The Associate Director , RACMC Portfolio Products, will be responsible for ... and executing post-approval Regulatory CMC strategies, reviewing CMC information and data , authoring CMC submissions, and interacting with Health Authorities to meet… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Development on Project Teams. ResponsibilitiesStudy Strategy: Provides the strategic direction to Biostats Data Mgmt & Data Ops for EDC, edit checks, data ... appropriate biomarker, PK / PD measurements; Reviews emerging clinical data regularly; Leads dose-escalation meetings; Performs quality assessment with Delivery… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Safety Pharmacovigilance (CSPV) leads in the maintenance of Company Core Data Sheets (CCDS) for assigned products. This position drives/leads the maintenance ... all applicable regulations and guidelines and with Company Core Data Sheets and manages deviations. This position interacts across...either the US or EU. Preparation of updated Core Data Sheets, and EU and US Documentation: Independently manages,… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …in class sourcing and procurement for Global RD - for their specific categories.- Data Analysis Based Decision-Making- Uses rigorous analyses of data as well as ... knowledge of clinical trials preferred- Demonstrated ability to leverage digital data and analytics preferred- Demonstrated ability driving or participating in… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …to study team on all aspects of statistical activities; collaborates closely with data manager to ensure high quality data .Drug Development Strategy: Provides ... input to multiple aspects of the development plan to ensure the study designs at each phase of the development are scientifically sound, can fulfill regulatory requirements and deliver the pre-specified product profile.CRO / Vendor Oversight: Review CRO/vendor… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …guidance to study team on all aspects of statistical activities; collaborates closely with data manager to ensure high quality data . Work closely with internal ... statistical programmer.Drug Development Strategy: Provides input to multiple aspects of the development plan to ensure the study designs at each phase of the development are scientifically sound, can fulfill regulatory requirements and deliver the… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …functions include: Clinical Operations, Clinical Development, Biostatistics and Data Management, Regulatory Affairs, Quantitative Clinical Pharmacology, Clinical ... reuse. Maintains detailed Solution Architecture diagrams for ALL systems, integrations, and data flows. Work with the Enterprise Architecture team to ensure all… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …the Daiichi Sankyo organization to obtain and/or provide information/ data for regulatory filings.Review and interpret regulatory guidelinesContinuing Education: ... Keep current with regulations and guidance documents; attend meetings, seminars, conferences on relevant topics; read journals, newsletters, scientific papers; research the answers to RA questions. Qualifications: Successful candidates will be able to meet the… more
