Principal Statistical Programmers

SuperStaff

Metro Manila, Philippines Remote permanent

Posted: February 8, 2026

Quick Summary

We are looking for experienced statistical programmers to work with one of our clients in Metro Manila, Philippines. The ideal candidate should have experience in working on Oncology TA and be able to lead a team of 2-4 members. The role involves conducting programming activities, leading a study team, and migrating data from legacy datasets to standards such as CDISC.

Required Skills

Job Description

We are looking for experience Statistical Programmers to work with one of our clients.

Job Responsibilities

• Working under the direction of the Team Lead / Project Manager, the senior statistical programmer conducts programming activities for a trial, early phase project, indication, or publication activities.

• Lead at least one study team in terms of providing technical and domain-related guidance.
• May required to lead and manage a team of 2-4 members
• Experience of working on Oncology TA is mandatory.
• Ability to work on data migration from legacy datasets to standards such as CDISC or any other client-specific standard.
• Read and understand the program specifications document.
• Prepare SAS analysis datasets, tables, listings, and figures as per specifications.
• Create programs to create graphs and tables that are required in CSRs, safety reports, efficacy reports, etc. ensuring on-time quality delivery.
• Validate and transform datasets as per client assignment specifications.
• Validate tables, listings, and figures as per client assignment specifications.
• Coordinate with the client and US team for clarity of specifications, data issues, outliers, reviews, schedules, etc.
• Contribute in the organization’s recruitment process by identifying needs and required skill sets of resources and conducting interviews to hire appropriate resources.
• Perform all the above tasks using standard operating procedures (SOPs) as defined in the Quality Management System or the respective client(s) as applicable

Requirements:
• BS or MS degree in Computer Science, Statistics, or related health science field with a minimum of 5 years of SAS programming experience with clinical trial data.
• Well-conversed with regulatory requirements and drug development process.
• Good understanding of the Clinical trial domain and good SAS programming skills
• Ability to work independently.

Benefits:
• HMO with 1 free dependent upon hire
• Life Insurance
• 10% Night Differential
• 20 PTO credits annually
• VL and SL cash conversion
• Annual Performance-Based Merit Increases and Employee Recognition
• Great Company Culture
• Career Growth and Learnings
• Night Shift
• Work from Home

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