Senior Statistical Programmer Lead Global Hybrid

Merck & Co.; North Wales (Montgomery County); Hybrid; USD 117,000 - 184,000; Full time

Job summary

Merck & Co., Inc. seeks aSenior SAS Programmer in the US to support late-stage clinical development projects. You will lead programming tasks, develop analysis datasets, and deliver tables, listings, and figures for regulatory submissions.

Responsibilities include coordinating a global programming team, ensuring quality and timeliness, and collaborating with statisticians and other stakeholders throughout the product lifecycle. Hybrid work arrangement.

Qualifications

• BA/BS or MS in a related field with SAS programming experience in clinical trials.
• Experience in CDISC ADaM and statistical analysis for regulatory submissions.
• Strong interpersonal, written, and presentation skills.

Responsibilities

• Lead statistical programming for late-stage drug/vaccine projects.
• Develop and validate analysis datasets, tables, listings, figures.
• Design programming datasets and collaborate with stakeholders.
• Coordinate global programming team and outsource staff.

Skills

SAS programming

Statistical analysis

CDISC ADaM

Data management concepts

Clinical trial programming

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/MACRO

SAS/GRAPH

CDISC standards

Job description

Merck & Co., Inc. seeks aSenior SAS Programmer in the US to support late-stage clinical development projects. You will lead programming tasks, develop analysis datasets, and deliver tables, listings, and figures for regulatory submissions.

Responsibilities include coordinating a global programming team, ensuring quality and timeliness, and collaborating with statisticians and other stakeholders throughout the product lifecycle. Hybrid work arrangement.