-
Labeling reviewers and Regulatory Authorities. Prepare comparison tables for labeling team discussions. Edit and format labeling documents- Ensure the document complies with the appropriate template (e.g
-
in accordance with agreed upon timelines. Contribute to the training of colleagues on quality standards and processes. Develop and sustain constructive relationships within other Pfizer lines including
-
statistical deliverables on assigned projects, including timeliness and quality of deliverables according to project plans. Develop effective collaborations with others within clinical teams, partner lines
-
processes and maintain compliance with applicable policies. Provide project management oversight of designated vendors on system design projects and other enhancement projects or initiatives. Develop
-
diverse leadership experiences and capabilities including: the ability to influence and collaborate with peers, develop and coach others, oversee and guide the work of other colleagues to achieve meaningful
-
nonclinical safety studies. Provide critical experimental design input for in vivo and in vitro studies. Develop automated statistical solutions to increase the efficiency of DSRD study conduct and reporting
-
Team to develop and maintain Core Data Sheets (CDS), United States Package Inserts (USPI), Summary of Product Characteristics (SPC) for products registered in the EU via the Centralized, Mutual
-
independently on project teams, although, may need instruction on more complex or unusual study challenges and/or tasks. Serve as technical support for clinical issues raised by internal and external
-
channels, driving improved education, clinical/business decision making, and impactful patient outcomes globally. Through innovative technologies and medical insights, the team will optimize existing
-
Will Achieve You will help Pfizer develop and implement chemistry, manufacturing and control (CMC) regulatory strategies for large molecules and antibody-drug conjugates to meet global regulatory