Senior Statistical Programming Lead (Hybrid)

MSD Malaysia; North Wales (Montgomery County); Hybrid; USD 142,000 - 224,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

401(k) retirement plan

Paid holidays

Job summary

Merck invites a senior Statistical Programmer to lead programming activities across multiple clinical development projects. You will design and maintain analysis datasets, tables, listings and figures supporting regulatory submissions and post-marketing activities.

The role requires strong leadership, cross-functional collaboration and extensive SAS/ADaM experience in a global environment. Hybrid work arrangements and a comprehensive benefits package are available.

Qualifications

• BA/BS with minimum 9 years SAS programming in clinical trials.
• MS with minimum 7 years SAS programming in clinical trials.
• Excellent interpersonal, written and presentation skills.
• Experience in CDISC and ADaM standards; regulatory submissions.

Responsibilities

• Lead statistical programming for late-stage clinical projects.
• Develop and validate analysis datasets, tables, listings and figures.
• Coordinate global programming team including outsource staff.
• Ensure high-quality deliverables and timely execution across life cycle.

Skills

SAS programming

CDISC ADaM

Regulatory submissions

Stakeholder management

Project management

Education

Bachelor’s degree in Computer Science/Statistics/Life Sciences/Engineering or related

MS in related field

Tools

SAS software

Job description

Merck invites a senior Statistical Programmer to lead programming activities across multiple clinical development projects. You will design and maintain analysis datasets, tables, listings and figures supporting regulatory submissions and post-marketing activities.

The role requires strong leadership, cross-functional collaboration and extensive SAS/ADaM experience in a global environment. Hybrid work arrangements and a comprehensive benefits package are available.