Job Description

Role Summary: Design, analyze, and interpret clinical trials and/or observational studies in compliance with relevant regulatory requirements, standards and best practices. Provide statistical expertise and contributions for projects and protocols in support of clinical development under the supervision of senior statistical staff. Provide statistical expertise on regulatory submissions and ensure quality and appropriateness of submission deliverables under the supervision of senior statistical staff. Provide statistical expertise in maximizing the value of aggregate clinical data in support of scientific and drug development strategies under the supervision of senior statistical staff. Provide study level statistical expertise and communicate resource needs to management and other line functions for the execution of statistical tasks. Basic Qualifications: Advanced degree (Masters, PhD) in Statistics, Biostatistics, or related field. 3-5 yrs. of relevant experience in clinical trials is desirable but not necessary. 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. Working knowledge of SAS, R Location:Chennai Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.Medical#LI-PFE

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