23 Design Manager positions at Pfizer in New-York

Manager, Biostatistics

cutting edge design and process development capabilities to accelerate and bring the best in class medicines to patients around the world. POSITION SUMMARY You will represent Biostatistics on cross

Trial Master File Operations, Senior Manager

the acquisition and divestiture of TMF contentwhile developing repeatable efficient process for TMF in integrations Lead design and execution of remediation projects and improvement projects Configure Study

Associate Director, Program Manager - Vaccines Development

cutting edge design and process development capabilities to accelerate and bring the best - in - class medicines to patients around the world. What You Will Achieve In your role, you will be at the center

Senior Manager, Data Science and AI

and will either support a brand or therapeutic area or be part of a team designing, delivering, and upgrading innovative capabilities . This includes leading the execution and interpretation of AI/ML

Study Operations Manager II

. Accountable for the execution of tasks and developing solutions to problems as needed to support deliverables. The Study Operations Manager will be fully accountable and responsible for tasks as designated

Manager, R&D Compliance Operations

of designated vendors on system support projects and will oversee the development of core communications, SOPs, and/or colleague training materials. Individual project work to meet the team's semester-based goals

Sr Manager, GCP Auditor

improvements Exhibits good project management capabilities Has domain expertise in 2 or more technical areas Ability to work with ambiguity and adapt plan when needed Experience evaluating and understanding

Vaccine Asset Planner (Manager), Project Management & Continuous Improvement

cutting edge design and process development capabilities to accelerate and bring the best - in - class medicines to patients around the world. What You Will Achieve The Vaccine Asset Planner (Manager

Manager, Clinical Scientist

collaboratively with Sr. Manager and/or Lead Clinical Scientists, and Study Clinicians to provide CS support to moderately complex tasks within the categories of: 1) protocol and study design, 2) data review and

Senior Manager, Regulatory Affairs CMC

and internal quality procedures. Investigate opportunities for regulatory innovation / promote the use of novel approaches within project teams to resolve issues and problems. Develop effective