Hybrid Statistical Programmer: Early-Stage Oncology

MSD

Pennsylvania

Hybrid

USD 96.000 - 151.000

Vollzeit

Vor 3 Tagen
Sei unter den ersten Bewerbenden

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

Schaffe es an den ATS-Filtern vorbei

Benefits dieser Stelle

Hybrid work model
Annual bonus
Long-term incentive

Zusammenfassung

MSD is seeking a Scientist, Statistical Programming to support early-stage oncology programs in a hybrid work model (Pennsylvania/NJ). You will develop, validate, and maintain analysis datasets, tables, listings, and figures under supervision, ensuring high quality deliverables for regulatory submissions.

The role requires SAS programming experience in clinical trials, knowledge of CDISC ADaM/SDTM, and collaboration with project teams and external vendors.

Qualifikationen

  • BA/BS in a related field plus 2 years SAS programming experience in a clinical trial environment
  • MS in a related field is preferred
  • Experience with SDTM and ADaM preferred

Aufgaben

  • Develop, validate, and maintain efficacy and safety datasets, tables, listings, and figures at a protocol level
  • Ensure deliverable quality and compliance with SOPs and programming standards
  • Collaborate with project teams and outsource provider staff on reporting deliverables

Kenntnisse

SAS programming
CDISC ADaM
SDTM
Statistical programming
Data management
Interpersonal communication
Negotiation
Unix
R programming

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
R

Jobbeschreibung

MSD is seeking a Scientist, Statistical Programming to support early-stage oncology programs in a hybrid work model (Pennsylvania/NJ). You will develop, validate, and maintain analysis datasets, tables, listings, and figures under supervision, ensuring high quality deliverables for regulatory submissions.

The role requires SAS programming experience in clinical trials, knowledge of CDISC ADaM/SDTM, and collaboration with project teams and external vendors.

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