ROLE SUMMARY

• 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.

ROLE RESPONSIBILITIES

• Provide statistical input to study designs, statistical analysis plans, interpretation of statistical results, project development plans, regulatory issues and scientific and commercialization projects

• Provide planning, delivery and communication of statistical analyses, data presentations, and scientific reports, including clinical trial results, exploratory and meta-analysis results, support for publication activities, scientific presentations.

• Accountable for study level statistical deliverables on assigned projects.

• Ensure that all study level statistical activities are conducted in compliance with relevant regulatory requirements and Pfizer standards.

• Provide statistical input to cross-functional activities – collaborate with other statisticians, study managers, and other colleagues – for assigned studies and regulatory submissions

• Ensure timeliness and quality of statistical deliverables according to project plans for assigned studies and projects.

• Comply with all statistics and quality processes and standards that are applicable to statistical outputs, and support processes that require statistical input.

• Participate in technical forums on statistical methodology and its applications pertinent to business needs.

• Help maintain a strong statistics community at Pfizer through collaborations, scholarship, presentations, and learnings across divisions.

This is an individual contributor role.

BASIC QUALIFICATIONS

• Advanced degree (Masters, PhD) in Statistics, Biostatistics, or related field.

• 5-8 yrs. of relevant experience for Masters level, entry level Ph.D. as long as the Ph.D. research work is in a relevant area

• Experience in clinical trials is necessary for Masters degree, desirable for Ph.D.

• Strong statistical skills with application to clinical trials.

• Effective verbal and written English communication skills in relating to colleagues and associates both inside and outside the organization

PREFERRED QUALIFICATIONS

• Working knowledge of SAS, R

  
 

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

Medical

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