Associate, Statistical Data Scientist

• 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 opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

Medical

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