Late-Stage Oncology Statistical Programming Lead (Hybrid)

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

Job summary

Merck & Co., Inc. in Rahway, NJ, seeks an Associate Principal Scientist, Statistical Programming, Late-Stage Oncology, to lead programming activities for complex late-stage projects.

You will design analysis datasets, tables, listings, graphs, and support global regulatory submissions across multiple trials. The role requires strong SAS programming expertise, CDISC/ADaM familiarity, and the ability to manage a global team in a hybrid work environment.

Qualifications

• BS or MS in a quantitative field with clinical trial programming experience.
• Minimum 7–9 years SAS programming experience in a clinical trial environment depending on degree.
• Experience leading programming teams and coordinating global outsource providers.

Responsibilities

• Lead statistical programming activities for late-stage projects.
• Coordinate global programming team and maintain project plans.
• Ensure high-quality deliverables across trials and regulatory submissions.

Skills

SAS programming

Statistical programming

Leadership

Project planning

Education

BS in Computer Science/Statistics/Engineering

MS in related field

Tools

SAS

SAS/MACRO

CDISC/ADaM

Job description

Merck & Co., Inc. in Rahway, NJ, seeks an Associate Principal Scientist, Statistical Programming, Late-Stage Oncology, to lead programming activities for complex late-stage projects.

You will design analysis datasets, tables, listings, graphs, and support global regulatory submissions across multiple trials. The role requires strong SAS programming expertise, CDISC/ADaM familiarity, and the ability to manage a global team in a hybrid work environment.