Associate, Statistical Data Scientist (Chennai)

Bachelor or Master (preferred) Degree in Statistics, Computer Sciences, Engineering, Pharmacy, biological sciences, IT, or related field. - At least 2 years relevant experience in SAS or R programming and working knowledge of clinical trials. - Accountable for their assigned work supporting the standards/study deliverables - Contributes to over 80% of their time to programming deliverables assigned within the scope of the function in either SAS, R or Python. - Develop/Validate datasets, TFL as per CDISC aligned Pfizer Standards or Pfizer Data Standards for Study/Project/Portfolio (TA or Study Programming) - Explore the existing code base and execute/perform runs as required, also develop/modify as per the needs and specifications suggested to the standards team as appropriate - (Standards Programming) - Contribute to QC and validation plan suitable across Standards, Programming and Submissions. - Understand standard/study/project/portfolio requirements, specifications to gain deeper understanding of expectations and programming requirements. - Ensures appropriate documentation are completed for their deliverables with help of senior programmers. - Works with programming leads to ensure clear specifications for their programmed deliverables are in place. - Regularly update leads on progress and time estimations to ensure smooth daily operations and accurate planning Advances job knowledge to next level by participating/contributing in/to opportunities both globally and locally. Work Location Assignment: Hybrid Pfizer is an equal chance employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates. Medical LI-PFE .