Design, analyze, and interpret clinical trials and/or observational studies in compliance with relevant regulatory requirements, Pfizer standards, and best practices.
Provide statistical expertise and contributions for projects and protocols in support of clinical development.
Provide statistical expertise on regulatory submissions and ensure quality and appropriateness of submission deliverables.
Provide statistical expertise in maximizing the value of aggregate clinical data in support of scientific and drug development strategies.
BASIC QUALIFICATIONS
Advanced degree in statistics, biostatistics, or related field.
Capability to provide statistical leadership to cross -functional teams at the protocol level.
Strong statistical skills with application to clinical trials and/or analysis of observational studies
Effective verbal and written communication skills in relating to colleagues and associates both inside and outside the organization.
PREFERRED QUALIFICATIONS
At least 4 years of relevant clinical trial and business experience
Work Location Assignment: Flexible
#LI-PFE Work Location Assignment: Flexible
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.