Lead Scientist, Statistical Programming- Oncology (Hybrid)

MSD

Pennsylvania

Hybrid

USD 117.000 - 184.000

Vollzeit

14 Tage+

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Benefits dieser Stelle

Medical Insurance
Dental Insurance
Vision Insurance
401(k) Retirement Plan
Paid Holidays
Paid Vacation
Sick Leave

Zusammenfassung

Merck & Co., Inc. in Rahway, NJ: Hybrid Senior Scientist, Statistical Programming for Late-Stage Oncology. Lead analysis deliverables for trials and regulatory submissions, coordinating global programming teams to ensure timely, high-quality outputs.

The role requires strong SAS/ADaM/CDISC expertise, data management, and project leadership within a regulated R&D setting, with collaboration across statistics, safety and data management functions.

Qualifikationen

  • CDISC ADaM, CDISC standards and regulatory submissions experience.
  • Experience in data management, data modeling and numerical analysis.
  • SAS programming in a clinical trial environment; SDLC and waterfall model familiarity.

Aufgaben

  • Develop and validate analysis datasets, tables, listings and figures for trials.
  • Lead and coordinate a global programming team and outsource staff.
  • Ensure deliverables meet regulatory requirements and SOPs.

Kenntnisse

CDISC/ADaM
SAS Programming
Data Management
FDA Submissions
Project Management
Statistical Analysis
Stakeholder Mgmt
SDLC
Data Modeling
Waterfall Model

Ausbildung

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
Microsoft Project
Python
R
R Shiny

Jobbeschreibung

Merck & Co., Inc. in Rahway, NJ: Hybrid Senior Scientist, Statistical Programming for Late-Stage Oncology. Lead analysis deliverables for trials and regulatory submissions, coordinating global programming teams to ensure timely, high-quality outputs.

The role requires strong SAS/ADaM/CDISC expertise, data management, and project leadership within a regulated R&D setting, with collaboration across statistics, safety and data management functions.

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