Statistical Data Scientist
2 weeks ago
As a key member of our team at Pfizer, you will be responsible for delivering high-quality statistical programming deliverables to support clinical study teams. Your expertise in statistical programming and SAS will enable you to create analysis-ready datasets, tables, listings, and figures that meet the highest standards of quality and accuracy.
With a strong understanding of ICH and regulatory guidelines, you will ensure that all programming deliverables adhere to these standards. Your ability to work independently and with limited oversight will be essential in meeting tight deadlines and delivering results under pressure.
Key responsibilities will include:
- Developing and maintaining high-quality statistical programming deliverables
- Collaborating with statisticians and programming leads to ensure clear specifications for programmed deliverables
- Ensuring adherence to high-quality programming standards in daily work
- Contributing to department-level initiatives and staying up-to-date with industry developments
Qualifications and skills required include:
- Bachelor or Master's degree in Statistics, Biological Sciences, IT, or related field
- At least 6-8 years of relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency
- Statistical programming and SAS experience
- Clinical trials expertise with an understanding of data operations required for reporting clinical trial data
- Good understanding of ICH and regulatory guidelines
- Working knowledge of clinical data and relevant data standards
- Strong written and oral communication skills, and project management skills
- Proven ability to operate with limited oversight
- Knowledge of at least one Therapeutic Area
- Proven ability to manage delivery under tight timelines
- CDISC experience desirable
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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