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Protocol Intelligence
Data-driven signals on your job's competitivenessTier-1 employer and metro location increase applicants, but clinical/CDISC statistical programming specialization limits generalist competition.
Clinical trial and CDISC-centric expertise is industry-specific, limiting cross-industry transferability.
Regulated clinical context with mandatory CDISC and SAS/R/Python skills enforces strict, specialized hiring filters.
Job Description
Structured overview of role & requirementsAbout This Role
Deliver medium to high complexity statistical programming tasks independently, supporting study/project teams with datasets, TFLs, and standards alignment using SAS, R, or Python.
Ensure compliance with Pfizer's programming standards and processes, including documentation, quality control, and timely delivery within assigned scope.
Collaborate across stakeholders including clinicians and statisticians, contribute up to 80% time on programming deliverables and 20% on self-learning and development.
Minimum Requirements
Proficient in statistical programming languages such as SAS, R, or Python with demonstrated experience.
Experience handling medium to high complexity statistical programming deliverables independently in study or project contexts.
Ability to work collaboratively across multiple time zones and teams, with knowledge of CDISC and Pfizer-specific data standards.
Work Experience Required: Not explicitly mentioned in the JD.
Ideal Candidate Profile
Experienced individual contributor comfortable with independently managing programming tasks and stakeholder collaboration in clinical study environments.
Familiarity with core safety and therapeutic area specific data standards, able to lead development of standards as needed.
Demonstrates routine to complex problem solving skills with ability to update leadership and contribute to both global and local initiatives.