-
-term objectives. Organizational Relationships: Reports to US Vaccines Medical and Scientific Affairs Lead Will develop a strong relationship with all cross functional team members related to respective
-
-term objectives. Organizational Relationships: Reports to US Vaccines Medical and Scientific Affairs Lead Will develop a strong relationship with all cross functional team members related to respective
-
Will Achieve You will help Pfizer develop and implement chemistry, manufacturing and controls (CMC) regulatory strategies for small and/or large molecules to meet global regulatory requirements
-
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
-
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
-
Will Achieve You will help Pfizer develop and implement chemistry, manufacturing and controls (CMC) regulatory strategies for small and/or large molecules to meet global regulatory requirements
-
ROLE SUMMARY The Director, Vaccine Market Access Analytics needs to utilize their extensive US Vaccines marketplace knowledge to develop analysis from the Pfizer and Customer perspective
-
publication activities , scientific presentations, and support to product defense. Accountable for timeliness and quality of study/submission level statistical deliverables on assigned projects. Develop
-
when appropriate to ensure customers are educated on the clinical and economic value of Pfizer medicines. ROLE RESPONSIBILITIES Assume the role of the foremost authority on matters concerning the Payer
-
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