Principal Statistical Programmer

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.