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The Role
Develop and deliver analysis-ready datasets, tables, listings, and figures for clinical studies using statistical programming. Ensure high-quality code, documentation, and QC; collaborate with statisticians and leads; apply ICH and regulatory standards and clinical data standards to support study and asset-level deliverables.
Summary Generated by Built In
Job Description
A productive, hands on programmer who applies technical knowledge and practical experience to deliver statistical programming deliverables to support assets and study teams with limited supervision early in role and independently later in role.•
Ensures excellence in the programming of analysis ready datasets, tables, listings, and figures for which they are responsible•
Ensures adherence to high quality programming standards in their daily work. Accountable for the quality and timely delivery of datasets and displays required for their clinical study reports as well as other asset level deliverables they may be programming.
Ensures appropriate documentation and QC across the lifespan of the study for all of their programming deliverables.
Exhibits routine and occasionally complex problem solving skills, seeking direction when appropriate.•
Works with statisticians and programming leads to ensure clear specifications for their programmed deliverables are in place.
Will be knowledgeable in core safety standards as well as TA standards pertinent to their project, may aid in development of standards necessary for their study
May contribute to department level initiatives.
QUALIFICATIONS
Bachelor or Master (preferred) Degree in Statistics, Biological Sciences, IT, or related field.•
At least 3 years relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency.•
Statistical Programming and SAS hand-on experience•
Clinical trials expertise with an understanding of data operations required for the reporting of clinical trial data.•
Good understanding of ICH and regulatory guidelines•
Working knowledge of clinical data and relevant data standards
Work Location Assignment: Flexible
Work Location Assignment: Flexible
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.
To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers .
Medical
#BI-Hybrid
A productive, hands on programmer who applies technical knowledge and practical experience to deliver statistical programming deliverables to support assets and study teams with limited supervision early in role and independently later in role.•
Ensures excellence in the programming of analysis ready datasets, tables, listings, and figures for which they are responsible•
Ensures adherence to high quality programming standards in their daily work. Accountable for the quality and timely delivery of datasets and displays required for their clinical study reports as well as other asset level deliverables they may be programming.
Ensures appropriate documentation and QC across the lifespan of the study for all of their programming deliverables.
Exhibits routine and occasionally complex problem solving skills, seeking direction when appropriate.•
Works with statisticians and programming leads to ensure clear specifications for their programmed deliverables are in place.
Will be knowledgeable in core safety standards as well as TA standards pertinent to their project, may aid in development of standards necessary for their study
May contribute to department level initiatives.
QUALIFICATIONS
Bachelor or Master (preferred) Degree in Statistics, Biological Sciences, IT, or related field.•
At least 3 years relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency.•
Statistical Programming and SAS hand-on experience•
Clinical trials expertise with an understanding of data operations required for the reporting of clinical trial data.•
Good understanding of ICH and regulatory guidelines•
Working knowledge of clinical data and relevant data standards
Work Location Assignment: Flexible
Work Location Assignment: Flexible
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.
To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers .
Medical
#BI-Hybrid
Skills Required
- Bachelor's degree in Statistics, Biological Sciences, IT, or related field
- Master's degree (preferred)
- At least 3 years relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency
- Statistical programming and hands-on SAS experience
- Clinical trials expertise and understanding of data operations for clinical trial reporting
- Good understanding of ICH and regulatory guidelines
- Working knowledge of clinical data and relevant data standards
What the Team is Saying
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Pfizer Compensation & Benefits Highlights
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Healthcare Strength — Official materials describe comprehensive medical, dental, vision, and mental-health support, plus fertility/family‑building and transgender‑inclusive coverage; eligible Pfizer medications are noted as available at no cost in U.S. plans. Wellness resources such as telehealth and preventative programs are also emphasized.
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Retirement Support — Company documents highlight a 401(k) with matching contributions plus an additional Retirement Savings Contribution beyond the match. Financial planning support and company‑paid life and disability insurance further bolster long‑term security.
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Leave & Time Off Breadth — Corporate pages and job postings describe paid vacation and holidays, caregiver leave, and paid parental leave for both parents. Materials also note that details can vary by role and location.
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The Company
What We Do
Our purpose ensures that patients remain at the center of all we do. We live our purpose by sourcing the best science in the world; partnering with others in the healthcare system to improve access to our medicines; using digital technologies to enhance our drug discovery and development, as well as patient outcomes; and leading the conversation to advocate for pro-innovation/pro-patient policies.
Why Work With Us
We are the inventors, the problem solvers, the big thinkers — those who surmount any hurdle to deliver breakthrough medicines to the people who are counting on them the most.
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Pfizer Offices
Hybrid Workspace
Employees engage in a combination of remote and on-site work.
Typical time on-site:
2.5 days a week
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