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Sr. Scientist, Stat. Programming, Late-Stage Oncology; Hybrid

Job in Rahway, Union County, New Jersey, 07065, USA
Listing for: Merck
Full Time position
Listed on 2026-07-19
Job specializations:
  • IT/Tech
    Data Scientist, Data Analyst, Data Engineering
Salary/Wage Range or Industry Benchmark: 117000 - 184200 USD Yearly USD 117000.00 184200.00 YEAR
Job Description & How to Apply Below
Position: Sr. Scientist, Stat. Programming, Late-Stage Oncology (Hybrid)

In BARDS (Biostatistics and Research Decision Sciences), a distinguished department within our Company's renowned Research and Development division, quantitative scientists, in partnership with other subject matter experts, apply state‑of‑the‑art scientific methodologies and tools to enable the discovery, development, regulatory approval, manufacturing, and marketing of medical drugs and vaccines for the benefit of patients and global human health. This position supports statistical programming activities for late-stage drug/vaccine clinical development projects, including leadership of one or more projects.

The incumbent is responsible for the design and maintenance of statistical datasets that support multiple stakeholder groups and serves as the statistical programming point of contact throughout the product lifecycle.

Primary Activities
  • Effective analysis and report programming development and validation utilizing global and therapeutic area standards and following departmental SOPs and good programming practices
  • Maintain and manage a project plan including resource forecasting
  • Coordinate the activities of a global programming team that includes outsource provider staff
  • Membership on departmental strategic initiative team
Education and

Minimum Requirements
  • BA/BS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus a minimum of 5 years SAS programming experience in a clinical trial environment
  • OR
  • MS in Computer Science, Statistics, Applied Mathematics, Life Sciences, Engineering or related field plus a minimum of 3 years SAS programming experience in a clinical trial environment
Department Required Skills and Experience
  • Effective interpersonal skills and ability to negotiate and collaborate effectively
  • Effective written, oral, and presentation skills
  • Experience in developing analysis and reporting deliverables for R&D projects (data, analyses, tables, graphics, listings)
  • A project leader; completes tasks independently at a project level; ability to collaborate with key stakeholders
Position Specific Required Skills and Experience
  • Significant expertise in SAS and clinical trial programming including data steps, procedures, SAS/MACRO, SAS/GRAPH; systems and database expertise
  • Designs and develops complex programming algorithms
  • Ability to comprehend analysis plans which may describe methodology to be programmed; an understanding of statistical terminology and concepts
  • Familiarity with clinical data management concepts
  • Experience in CDISC and ADaM standards
  • Experience ensuring process compliance and deliverable quality
  • Strategic thinking – ability to turn strategy into tactical activities; design of statistical databases with the end in mind that optimize analysis and reporting and leverage departmental standards and industry best-practices
  • Ability to anticipate stakeholder requirements
Preferred Skills and Experience
  • Experience with GenAI tools (e.g., Python, R, R Shiny, Claude, etc.)
  • Demonstrated success in the assurance of deliverable quality and process compliance; strong working knowledge of reporting processes (SOPs) and software development life‑cycle (SDLC)
  • US and/or worldwide drug or vaccine regulatory application submission experience including the development of electronic submission deliverables
  • Experience assuring programming consistency across protocols and projects, directing the program development effort of other programmers; experience as a programming mentor
  • Ability and interest to work across cultures and geographies
  • Ability to complete statistical programming deliverables through the use of global outsource partner programming staff
  • Experience developing and managing a project plan using Microsoft Project or similar package
  • Active in professional societies
  • Experience in process improvement
Required Skills
  • Clinical Development
  • Clinical SAS Programming
  • Clinical Trials
  • Database Management Systems (DBMS)
  • Data Management
  • Data Modeling
  • Leadership
  • Project Development
  • Project Leadership
  • SAS BI
  • Stakeholder Relationship Management
  • Statistical Analysis
  • Statistical Programming
Preferred Skills
  • Oncology
  • Python (Programming Language)
  • R Programming
Equal Employment Opportunity

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