Senior Statistical Programmer - Late-Stage Oncology Remote

Merck & Co.

North Wales (Montgomery County)

Remote

USD 117,000 - 184,000

Full time

14 days+

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Benefits offered by this job

Annual bonus
Long-term incentive
Medical benefits
Remote work flexibility

Job summary

Merck & Co. is seeking a senior statistical programmer to support BARDS in late-stage drug/vaccine clinical development projects.

You will lead statistical programming activities, develop and validate analysis datasets, tables, listings, and figures across trials and regulatory submissions. The role involves coordinating a global programming team, designing complex programming algorithms, ensuring quality and compliance with CDISC/ADaM standards, and collaborating with stakeholders to meet

Qualifications

  • BA/BS or MS with SAS programming experience in a clinical trial environment.
  • Experience designing and maintaining analysis datasets; familiarity with CDISC/ADaM standards.

Responsibilities

  • Lead statistical programming activities for late-stage drug/vaccine development projects.
  • Develop and validation of analysis datasets, tables, listings, and figures for trials and regulatory submissions.
  • Coordinate activities of a global programming team including outsource providers; ensure timely, high-quality deliverables.
  • Serve as statistical programming point of contact through product lifecycle; collaborate with stakeholders to meet project goals.

Skills

SAS programming
Clinical trials
SAS/MACRO
CDISC/ADaM
Leadership
Global collaboration

Education

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

Tools

SAS
Microsoft Project

Job description

Merck & Co. is seeking a senior statistical programmer to support BARDS in late-stage drug/vaccine clinical development projects.

You will lead statistical programming activities, develop and validate analysis datasets, tables, listings, and figures across trials and regulatory submissions. The role involves coordinating a global programming team, designing complex programming algorithms, ensuring quality and compliance with CDISC/ADaM standards, and collaborating with stakeholders to meet

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