Associate Statistical Programmer (Secondment - 6 Months)

Why Patients Need You

As an Associate Statistical Programmer within the Statistical Data Sciences and Analytics (SDSA) team you will play a critical role in supporting Pfizers global and regional clinical studies. Your expertise in SAS and R programming will help transform clinical data into meaningful insights that support regulatory submissions scientific publications and commercialization efforts.

What You Will Achieve

You will collaborate closely with statisticians and cross-functional teams to ensure the accuracy compliance and efficiency of clinical data reporting ultimately contributing to improved patient outcomes.

How You Will Achieve It

• Provide technical expertise and perform programming activities to support clinical trial data reporting.

• Design and implement statistical algorithms and code in alignment with Pfizers Systems Development Life Cycle (SDLC) programming standards and regulatory guidelines.

• Ensure all programs and outputs comply with ICH requirements and Pfizer SOPs.

• Deliver statistical analyses tables listings and graphs for integrated scientific reports and publications.

• Contribute to the planning and development of project deliverables ensuring timely and high-quality outputs.

• Support global strategies and standards to enable efficient integrated data analysis across studies and submissions.

• Maintain clear and timely communication with stakeholders to drive continuous improvement.

• Collaborate with managers and business owners to prioritize tasks and assess workload.

• Provide feedback on process efficiency and suggest improvements to enhance productivity.

Qualifications

Must-Have

• Experience supporting regulatory submissions and understanding clinical and regulatory operations.

• Proficiency in SAS and/or R programming languages.

• Familiarity with Windows OS MS Word Excel and Outlook.

• Strong analytical skills and attention to detail.

• Ability to manage multiple projects simultaneously and work within a matrix organization.

• Effective verbal and written communication skills in English.

Nice-to-Have

• No experience required

• Experience with structured SDLC environments and global reporting standards.

• Demonstrated ability to write clear standardized and well-documented programs.

• Experience presenting to both scientific and non-scientific audiences.

• Strong collaboration skills and ability to work in multicultural teams.

• Commitment to continuous learning and innovation in clinical programming.

• Willingness to challenge practices and contribute to a learning organization.

Other Job Details

• Last Date to Apply for Job:July 29 2025

• Additional Location Information:NO

• Eligible for Relocation Package NO

• Secondment 6 months

• If you are currently in a driving position with a fleet vehicle and this secondment does not require driving as an essential function of the position for12 months or longer you will be required to turn in your fleet vehicle for the duration of the non-driving secondment. Please refer to the Fleet Policy and Procedures document for more information.

• There will be no change to your current work location.

• Position is considered Flexible and colleagues are expected to comply with Log In For Your Day(LIFYD) requirements at site location (e.g. about 2.5 days a week in office).

Relocation assistance may be available based on business needs and/or eligibility.