Lead Statistical Programmer - Oncology (Contract)

Valtera Group Ltd; United States; On-site; USD 150,000 - 190,000; Full time

Job summary

Valtera Group Ltd. is seeking an experienced Lead Statistical Programmer for an initial 6-month contract in the United States. The role is hands-on, requiring independence, fast ramp-up, and a focus on regulated programming, CSR delivery and submission-ready data packages.

You will lead programming across multiple oncology studies, while staying hands-on with SAS and CDISC standards. Key responsibilities include owning timelines, validating SDTM/ADaM outputs, and coordinating with CROs and

Qualifications

• Extensive hands-on SAS programming in biotech/pharma settings.
• Strong SDTM/ADaM and TLF/TLG deliverables experience.
• Experience leading programming for clinical studies, especially in oncology.

Responsibilities

• Lead programming across 1–4 clinical studies.
• Remain hands-on in SAS and validate SDTM/ADaM outputs.
• Support CSR submission-ready data packages and regulatory deliverables.
• Review CRO datasets and outputs; manage validation and approvals.
• Collaborate with Biostatistics, Data Management and Clinical Operations.
• Own timelines and communicate risks early to protect milestones.

Skills

SAS programming

SDTM/ADaM

Oncology trials

CSR submission

Pinnacle 21

CDISC validation

Regulatory environment

Leadership/ownership

Timelines management

Tools

Pinnacle 21

Job description

Valtera Group Ltd. is seeking an experienced Lead Statistical Programmer for an initial 6-month contract in the United States. The role is hands-on, requiring independence, fast ramp-up, and a focus on regulated programming, CSR delivery and submission-ready data packages.

You will lead programming across multiple oncology studies, while staying hands-on with SAS and CDISC standards. Key responsibilities include owning timelines, validating SDTM/ADaM outputs, and coordinating with CROs and