Fulltime | Remote
We are seeking a highly skilled Principal Statistical Programmer to join our team. Reporting to the Team Lead or Project Manager, you will play a pivotal role in clinical trial programming, particularly within Oncology Therapeutic Areas (TA). You will lead study teams, ensure high-quality deliverables, and contribute to technical and domain-related guidance.
Key ResponsibilitiesConduct programming activities for trials, early-phase projects, indications, or publication-related tasks.
Lead at least one study team, providing technical guidance and domain expertise.
Manage and mentor a small team of 2–4 members as required.
Work on data migration from legacy datasets to CDISC standards or client-specific formats.
Review and interpret program specifications to prepare SAS analysis datasets, tables, listings, and figures.
Create programs for generating graphs and tables for CSRs, safety reports, efficacy reports, and other study deliverables, ensuring on-time and high-quality output.
Validate and transform datasets, tables, listings, and figures according to client specifications.
Coordinate with clients and US-based teams to clarify specifications, resolve data issues, and manage timelines.
Contribute to the organization’s recruitment process by identifying skill needs and interviewing candidates.
Adhere to standard operating procedures (SOPs) within the Quality Management System or client-specific guidelines.
BS or MS degree in Computer Science, Statistics, or related health science field.
Minimum 5 years of SAS programming experience with clinical trial data.
Hands-on experience in Oncology Therapeutic Areas (TA) is mandatory.
Strong understanding of clinical trial processes and regulatory requirements.
Proven ability to work independently and as part of a collaborative team.
Excellent SAS programming skills and a solid grasp of clinical data standards (CDISC preferred).
Work on impactful oncology projects with leading industry clients.
Opportunity to lead and mentor a high-performing team.
Exposure to cutting-edge clinical trial data management and analysis practices.
Principal Statistical Programmer • Pasig, NCR, PH
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