- Daiichi Sankyo, Inc. (Bernards, NJ)
- …other research areas centered around rare diseases and immune disorders. JOB SUMMARYThe Associate Director , GMP QA Process Excellence is accountable to collect ... analyze quality related process, define strategies to lead to the development and implementation of quality improvement initiatives across the organization.This role… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …areas centered around rare diseases and immune disorders. SummaryReporting to the Senior Director , I&A, the Associate Director , Global Oncology Forecasting ... will drive creation of demand and revenue forecasts. The Associate Director is a dynamic member of the Global Oncology I&A Team and partners closely with Market… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …the Specialty Medicine Business Units and is responsible for executing business development opportunities across a range of categories designed to advance the ... require participation in supervising, training and developing entry-level business development professionals within the Global BD function (eg Fellow).Responsibilities-… more
- Merck & Co. (Rahway, NJ)
- …of decision-making at our company, this position offers an opportunity for the Associate Director to drive pipeline impact across therapy areas.This Associate ... on a continuous basis in decision making and driving pipeline impact. The Associate Director will perform job duties independently with minimal supervision… more
- Merck & Co. (Rahway, NJ)
- Job Description Associate Director of Product Management, Patient Insights Engine- We are seeking an Associate Director of Product Management in the ... supervision. In this role, you will report into the Director of Product for PIE. You will seek to...Translating user needs into detailed product requirements for the development team. Collaboration with cross-functional teams: Working closely with… more
- Merck & Co. (Rahway, NJ)
- …the Quantitative Pharmacology and Pharmacometrics - Immune/Oncology (QP2-IO) team in the role of Associate Director QP2-IO team is part of the Global Clinical ... Development organization and has oversight over drug ...effective communication skills. As a subject matter expert, the Associate Director within the QP2-IO Group will… more
- Merck & Co. (Rahway, NJ)
- …partners with the Clinical Trial Operations teams within the Research & Development division to create, develop, and enhance innovative solutions to complex problem ... Driving License:NoHazardous Material(s):n/aRequired Skills:Asset Management, Benefits Management, Management System Development , Product Management, Requirements Management, Stakeholder Relationship Management, Strategic… more
- Merck & Co. (Rahway, NJ)
- …continue to be one of the world's biggest investors in Research & Development .- -The vision for the Global Workplace and Enterprise Services (GWES) organization is ... to improve patient's lives by providing world-class facility services & solutions that enable innovative research, medicines, & vaccines.- We deliver critical building and site services, including facility management, emergency response, utilities (including… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …of regulatory document. Collaborates as team member with AROs/CROs. Drafts development plans, protocol profiles, and sections of submission documents under guidance ... medical and/or scientific direction to Clinical Operations. Represents Clinical Development on Project Teams. ResponsibilitiesStudy Strategy: Provides the strategic… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …with some supervision. This position contributes to specific aspects of drug development plans with minimal supervision and contributes to documents submitted to ... works under some supervision to solve complex study problems.Responsibilities- Protocol Development , Case Report Form (CRF; review), Statistical Analysis Plan (SAP),… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …complexity including post marketing projects and those involving 3rd party development . This position partners with GRLs and Clinical Safety Pharmacovigilance (CSPV) ... may assist another Global Labeling Lead by managing labeling development or approval for either the US or EU....may assist another Global Labeling Lead by managing labeling development or approval for either the US or EU.Ensure… more
- Merck & Co. (Rahway, NJ)
- …valued colleagues across our Company enterprise.- - - Position Description - The Associate Director is responsible for identifying and driving improv ements to ... one of the world's biggest investors in Research & Development . - - The vision for the Global Workplace...both office personnel and research operations . - The Associate Director will serve as a key… more
- Merck & Co. (Rahway, NJ)
- Job Description Position Description: Associate Director , Financial Evaluation & Analysis (FE&A) Primarily responsible for all aspects of financial evaluation ... inputs, as well as interface with project leaders from Corporate Development , Corporate Licensing and Business Development .Estimate the financial impact… more
- Merck & Co. (Rahway, NJ)
- …professional to join the Global Safety Center of Excellence (CoE) team as an Associate Director , Safety Programs CoE.- This individual will be responsible for ... skills and excellence in Project Management.Experience in both strategy development and tactical execution.Experience in organizational change management (transformation)… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …The project teams will be defined based on the project needs and the respective development stage of the project. The CMC Lead will support the Sr. CMC Lead on ... Responsibilities - Accountability to lead teams within overall CMC development project(s), to support Sr CMC Lead. In case...strategies and activities for early and late phase drug development candidates within the team to support overall CMC… more
- Merck & Co. (Rahway, NJ)
- …the 'end-to-end' integrated clinical supply chain across the full our Research & Development Division portfolio of clinical trial s .- GCS is accountable for the ... The GCS Planning (Planning) organization is the key interface between clinical development teams and the operational/executional arms within the business.-- - - The… more
- Merck & Co. (Rahway, NJ)
- …journey to become the premier "Data First" commercial biopharma organization.In this Associate Director Data Product Management role, you will be part ... data product, including use case identification, discovery all the way to development and maintenance.Knowledge about specialty products, SP and Hub data and… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …objective setting sessions, Mid-Year Assessments, Year-End Assessments. Leads an employee development planning with each direct report. Sustains the payroll staff by ... recruiting, selecting, orienting, and training employees. Qualifications: Successful candidates will be able to meet the qualifications below with or without a reasonable accommodation. Education Qualifications (from an accredited college or university)-… more
- Merck & Co. (Rahway, NJ)
- …colleagues, and GSMG Process, Operations & Strategy (PO&S), and Supplier Development & Performance Management (SD&PM) to ensure effective management and reporting ... skills.Proven experience in large-scale organizational change initiatives.Expertise in strategy development and implementation.Cultural awareness and experience working within diverse,… more
- Merck & Co. (Rahway, NJ)
- Job DescriptionThe Associate Director of Scientific Nomenclature and Reference Data is responsible for assigning accurate chemical nomenclature to small ... IUPAC and CAS standards and rulesReference DataUtilizing knowledge of the drug development process and of master data principles for small molecules, biologics,… more
