- Bachelor or Master (preferred) Degree in Statistics, Computer Sciences, Engineering, Pharmacy, b iological s ciences, IT, or related field.
- At least 2 year s relevant experience in SAS or R programming and working knowledge of clinical trials.
- Accountable for their assigned work supporting the standards/s tudy 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.
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