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About the Role

Performs statistical duties related to clinical trials and regulatory submission documents for vaccine projects. Specializing in vaccine projects, provides statistical services for all regulatory submission documents, including clinical trial reports, and manages the quality control of statistical analysis plans. Offers statistical advice on development plans and protocols as a statistical representative. Supports programming tasks as needed. Leverages direct reporting to Global Vaccine Research, collaborating with Development Japan (DJ) through global communication (phone, email).

Responsibilities

Create and quality control statistical analysis plans.
Provide statistical advice on development plans and protocols.
Support programming tasks as needed.
Collaborate with Development Japan (DJ) through global communication.

Requirements

Minimum 5 years of experience in statistical work within clinical development, including creating statistical analysis plans.
Experience in vaccine development is desirable.
Willingness to work on vaccine development is desirable.

Skills

English proficiency (reading and writing: intermediate, conversation: intermediate)
TOEIC score of 600 or higher
SAS/R programming skills
Biostatistics training (e.g., BioS)

Location

Hybrid

Work Type

Hybrid

Experience Level

5+ years

About the Company

Pfizer careers are like no other. In our culture of individual ownership, we believe in our ability to improve future healthcare, and potential to transform millions of lives. We’re looking for new talent to join our global community, to unearth new innovative therapies that make the world a healthier place.

Equal Opportunity

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers.