Clinical Statistician

5 days ago

Chennai, India Pfizer Full time

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.
- 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

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