India – Chennai

ROLE SUMMARY

• Design, analyze, and interpret clinical trials and/or observational studies in compliance with relevant regulatory requirements, 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.
• 3-6 yrs 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.

PREFERRED QUALIFICATIONS

• Working knowledge of SAS, R

Apply here: https://pfizer.wd1.myworkdayjobs.com/en-US/PfizerCareers/job/India—Chennai/Clinical-Statistician_4913183?q=clinical&source=linkedin&locations=e2d3979e3af101936db42457076cbe8e&locations=e2d3979e3af1014c8c757857076c0e8f