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