Senior Associate, Principal Statistical Data Scientist
3 days ago
In this role, you will play a key part in supporting the development and implementation of statistical programming standards and processes.
You will work closely with the study teams and stakeholders to ensure that all deliverables are of high quality and meet the required standards.
"},{"title":"Key Responsibilities","content":"
Key Responsibilities:
- Develop and maintain statistical programming standards and processes.
- Collaborate with study teams and stakeholders to ensure high-quality deliverables.
- Contribute to the development and implementation of clinical data standards.
- Work with global stakeholders to ensure the completion of project goals and milestones.
Qualifications / Skills:
- Bachelor or Master (preferred) Degree in Statistics, Computer Sciences, Engineering, Pharmacy, biological sciences, IT, or related field.
- At least 5 - 6 years relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency.
- Understanding of clinical data and drug development process, CDISC standards required.
- Statistical Programming and SAS hand-on experience.
- Clinical trials expertise with an understanding of data operations required for the reporting of clinical.
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Work Location Assignment: Flexible
"}-
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