Principal Statistical Programmer
- Remote, Pasig, PH
- Research and Development
- Full-time
- Science & Research
- Master's Degree
- Mid-Senior level
- 40 - 40 hours per week
Principal Statistical Programmer
Fulltime | Remote
About the Role
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 Responsibilities
-
Conduct 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.
Qualifications & Experience
-
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).
- Remote work readiness, including a stable internet connection with minimum 100 Mbps speed.
Why Join Us
-
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.