Senior SAS Programmer: Lead Clinical Data & Submissions

WCG; United States; Presencial; USD 105.000 - 128.000; Tempo integral

Benefícios oferecidos por esta vaga

Health insurance

401(k) matching

Tuition reimbursement

Paid holidays & vacation

Career development opportunities

Resumo da vaga

WCG seeks a Senior Statistical Programmer to develop and validate SAS programs for regulatory submissions. You will lead programming activities, manage timelines, and mentor junior staff across cross-functional teams to ensure high-quality deliverables.

The role requires CDISC SDTM/ADaM expertise, strong SAS and macro skills, and 5+ years in pharma/biotech settings. Excellent communication and attention to detail are essential for success.

Qualificações

• Master's degree required in statistics, CS, mathematics, life sciences, or related field.
• Minimum 5 years SAS programming experience.
• 2 years macro programming experience required.
• 3+ years in pharmaceutical/biotech/medical device industry.
• CDISC data standards experience (SDTM/ADaM).
• Strong knowledge of SAP programming specifications.

Responsabilidades

• Develop, validate, and document SAS programs for clinical trial datasets and outputs for regulatory submissions.
• Lead programming activities, manage resources, timelines, and priorities.
• Perform QC checks and peer code reviews on all deliverables.
• Collaborate with statisticians, data managers, and clinical teams to ensure requirements are met.
• Troubleshoot data and programming issues; ensure accurate reporting.
• Coordinate multiple projects and adapt to evolving priorities.
• Mentor junior programmers on industry standards and best practices.

Conhecimentos

SAS programming

R programming

Macro programming

CDISC standards

SAP specs

Pharma industry

Clinical trials

Attention to detail

Formação

Master's degree in Statistics, Computer Science, Mathematics, Life Sciences, or related field

Descrição da vaga

WCG seeks a Senior Statistical Programmer to develop and validate SAS programs for regulatory submissions. You will lead programming activities, manage timelines, and mentor junior staff across cross-functional teams to ensure high-quality deliverables.

The role requires CDISC SDTM/ADaM expertise, strong SAS and macro skills, and 5+ years in pharma/biotech settings. Excellent communication and attention to detail are essential for success.