42 master Manager positions in United States

Senior Manager, Regulatory Affairs CMC

documentation systems Nice-to-Have Master's degree Experience engaging in the external regulatory and pharmaceutical environment 2+ years of hands-on CMC authoring experience (investigational, initial

Site Care Partner (Senior Manager)

Role Summary The Site Care Partner is the main Pfizer point of contact for investigative sites, responsible for building and retaining relationships from site activation through the lifecycle

Manager, PI Historian SME

projects to expand and maintain the system. Collaborating with the Infrastructure lead on strategy, methodologies, master planning and documentation of the PI data historian to align with industry best

Senior Manager, Financial Modeling Specialist, Market Access Analytics

, & PowerPoint PREFERRED QUALIFICATIONS MBA or master's level education Previous experience in managed markets analytics or a job function supporting the promotion of pharmaceuticals. Other Job Details: Last Date

Process Validation Manager

Will Achieve It Responsibilities include the following: Leading process validation activities: Defining PV strategies in a process validation master plan Generating protocols, evaluating data, and

Manager, Regional Regulatory Strategist

regulations Understand and can challenge scientific arguments, identifies regulatory scientific data needs and solves regulatory issues. Serve as primary contact to FDA (or other relevant regulatory authorities

Senior Manager, SAS Analytics & Insights

required in an analytical type function, which can include: consulting, primary quantitative market research, secondary data analysis, forecasting, predictive modeling. Understanding of the specialty

Sr. Manager, Process Automation (Manufacturing)

working to the overall plan, including management of and reporting. Support development of the Site Master Plan and Site Space Plan to ensure effective and strategic use of assets and capital investment

Senior Manager, Global Labeling Lead

deliverables remain on target to meet internal and external deadlines. The GLL serves as the GLM primary point of contact for Labeling Team members (e.g. Regulatory Strategist, Safety Risk Lead, Functional Line

Manager, Clinician (Non-MD), Early Clinical Development

ROLE SUMMARY Summarize the primary purpose & key accountabilities of the role, including geographical scope (i.e. Global vs. Country/Region). Summary should be concise and include strategic