- Daiichi Sankyo, Inc. (Bernards, NJ)
- …Executes statistical activities for low to medium complexity studies including study design , protocol development, CRF review , SAP development, analysis files ... Position Title: Senior Biostatistician Join a Legacy of Innovation 125...complexity studies including contributing to development of optimal study design , follow and execute statistical analysis plan and helps… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …system rejections or missing/incomplete data daily- Analyze various payment files; calculate, review , verify and post a variety of complex payroll data such as ... Analyze files submitted for completeness, audit updates to the payroll register, review state tax information for accuracy and appropriate processing, and establish… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …research areas centered around rare diseases and immune disorders.Summary The Senior Director sits within Global Oncology Clinical Development, an organization ... dedicated to the effective strategy, design , execution, and interpretation of Oncology clinical trials. Position...UAT (User Acceptance Testing) and CCG (CRF Completion Guidelines) review - Conducts clinical data review per Integrated… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …research areas centered around rare diseases and immune disorders. SummaryThe Senior Director sits within Global Oncology Clinical Development, an organization ... dedicated to the effective strategy, design , execution, and interpretation of Oncology clinical trials. Serves...Testing) and CCG (CRF Completion Guidelines) reviewConducts clinical data review per Integrated Data Review PlanAccountable for… more
- Merck & Co. (Rahway, NJ)
- …Description: Device Development Associate Principal Scientist - Development Strategy, Design Controls and Risk Management Our company's Device Development (DD) ... be responsible for leading and implementing medical device and combination product design controls and risk management activities for both new products and inline… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …addressed and managed appropriately. Ability to exercise influence at the senior leadership and/ or executive level wherever GLP/non-GLP/ research programs impacting ... sustainable improvements.Supports Regulatory Affairs in providing quality content and review of documents supporting GLP/non-GLP/ Research submissions to Health… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …lives for a living. Are you ready to make a difference? The Position As Senior Medical Director for the novel modalities team, you will be part of building, leading ... novel therapeutics Provide clinical and scientific expertise to the design of studies, writing of protocols and other study...as a leading member, or participant, at multiple internal review groups and utilize novel and creative methods to… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …typically a single non-pivotal trial (small size, standard complexity in design and geographic scope). Prepares clinical section of regulatory document. Collaborates ... Leads dose-escalation meetings; Performs quality assessment with Delivery Lead eg review Tables/Listings/Graphs before database lock and quality check of data; Works… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …personal development. Are you ready to maximize your potential with us? The Position The " Senior Architect - Data Management & AI" is a technical leader with a deep ... well as external suppliers and partners Essential Functions Lead evaluation, design , and analysis of enterprise-wide solutions Translate business and technical… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …immune disorders. Summary The Associate Director, Program Management is a senior position responsible for effectively planning, managing, and delivering multiple ... programs they manage. Program level responsibilities start with proactively partnering with senior leadership of the IT and the business community to identify and… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …personal development. Are you ready to realize your potential? The Position The Senior Specialist, EEO Investigations role will work under the supervision of EEO ... and affirmative action laws, regulations, concepts, and practices. Relationships The Senior Specialist, EEO Investigations role reports directly to the Associate… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …directors as well as cross functional partners. Relationships Reports to the Senior Director of HEOR Evidence Strategy and Synthesis within the Clinical Data ... RWE and Modelling teams, to ensure the strategic alignment from study design all the way through study communication to cross-functional stakeholders. Other… more
- Merck & Co. (Rahway, NJ)
- …or custom reports and presentations summarizing business and financial data for review by executives, managers, clients, and other stakeholders.-- Design and ... and internal clients such as marketing brand leaders, center of excellence teams, senior management etc., to stay abreast of business trends, understand the business… more
- Merck & Co. (Rahway, NJ)
- …and Biopharmaceutics, have 8-10 direct reports composed of experienced, senior and associate biopharmaceutic scientists.- The successful candidate will effectively ... and other functional areasExperience with regulatory submissions including writing / review of regulatory filings including INDs and NDAs.Must be innovative and… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …safety surveillance sub-function within the US East Coast Development Hub comprised of Senior Global Safety Leads, Global Safety Leads and Senior Global Safety ... adhering to company-wide policies, procedures and programs. Manages organizational design , structure, development, training and planning issues within sub-function.… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …excited about exploring the unknown? Does the idea of driving value through human-centered design pull you in? Are you ready to experiment with us? The Position The ... Identify opportunities for improvement within the customer campaigns and engagement. Review and interpret campaign/tactic data to inform adjustments on customer… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …excited about exploring the unknown? Does the idea of driving value through human-centered design pull you in? Are you ready to experiment with us? The Position The ... Identify opportunities for improvement within the customer campaigns and engagement. Review and interpret campaign/tactic data to inform adjustments on customer… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …across multiple functional areas. Relationships You will report to the Senior Director - Global Regulatory Portfolio Lead. Essential Functions Serve as ... mitigation plans to management and other internal stakeholders Perform regulatory review of all clinical and nonclinical documents for submissions, eg, clinical… more
- Port Authority of New York and New Jersey (New York, NY)
- …and rail transportation systems are important transportation links in the region. The Senior Design Executive org is part of a multi-discipline group of ... Office of the Chief Engineer and the Aviation Redevelopment Senior Design Executive, the Senior ...Chief Engineer, as needed. + Accountable for the interdisciplinary review of design and contract documents to… more
- City of New York (New York, NY)
- …Construction, Division of Public Buildings, Architecture and Engineering Unit seeks a Senior Design Reviewer (Mechanical) experienced in heating, ... for project scope development; existing conditions surveys and forensic analysis; the review of design and construction documents prepared by consultants; the… more
