Senior Statistical Programming Lead, Late-Stage Oncology

Merck; Rahway (NJ); Hybrid; USD 142,000 - 224,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

401(k) plan

Paid holidays

Job summary

Merck & Co., Inc. in Rahway, NJ is seeking a seasoned Statistical Programming Lead to drive late-stage drug/vaccine programs. You will develop analysis datasets, tables, listings, and figures, coordinating global teams and external outsource staff.

Requires 9+ years SAS programming in clinical trials (BA/BS) or 7+ years (MS). Strong collaboration, governance, and SDLC adherence are essential for successful regulatory submissions.

Qualifications

• BA/BS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus a minimum of 9 years SAS programming experience in a clinical trial environment
• MS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus a minimum of 7 years SAS programming experience in a clinical trial environment

Responsibilities

• Lead statistical programming activities for multiple and/or large/complex late-stage drug/vaccine clinical development projects.
• Develop and execute statistical analysis and reporting deliverables (datasets, tables, listings, figures).
• Design and maintain statistical datasets supporting multiple stakeholder groups.
• Collaborate with statistics and project stakeholders to ensure timely, high-quality deliverables.

Skills

Base SAS

SAS programming

Data management

FDA Submissions

Project management

Stakeholder management

Statistical programming

Clinical trials

Quality assurance

SAS macro

SAS/GRAPH

Education

BA/BS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field

MS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field

Tools

SAS

SAS Macro

SAS/GRAPH

Clinical Data Systems

Job description

Merck & Co., Inc. in Rahway, NJ is seeking a seasoned Statistical Programming Lead to drive late-stage drug/vaccine programs. You will develop analysis datasets, tables, listings, and figures, coordinating global teams and external outsource staff.

Requires 9+ years SAS programming in clinical trials (BA/BS) or 7+ years (MS). Strong collaboration, governance, and SDLC adherence are essential for successful regulatory submissions.