Senior Medical Statistician: Regulated Clinical Analytics

BD

Heber (UT)

Vor Ort

USD 90.000 - 130.000

Vollzeit

Vor 6 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

Medical benefits
Retirement plan
Paid time off
Parental leave
Education assistance
Commuter benefits

Zusammenfassung

BD is seeking a Statistician/Biostatistician to support product development, clinical studies, and business decisions in a regulated healthcare environment. You will design studies, develop analysis plans, analyze data, and communicate insights to cross-functional teams.

The ideal candidate holds a Master’s or PhD in Statistics or Biostatistics with experience in clinical research or regulated medical devices. Proficiency in R and/or SAS and ability to manage multiple projects is essential.

Qualifikationen

  • Master's degree in Statistics, Biostatistics, or related field.
  • Experience with clinical research or regulated healthcare environments.
  • Proficiency in programming using R and/or SAS.
  • Ability to manage multiple projects and communicate results.
  • Knowledge of reproducible research practices.
  • Familiarity with regulatory requirements.

Aufgaben

  • Design studies and analysis plans.
  • Analyze complex data and report findings.
  • Program and validate statistical code in R and/or SAS.
  • Collaborate with cross-functional teams.
  • Present findings to stakeholders.
  • Support regulatory submissions.

Kenntnisse

Statistics
Biostatistics
R programming
SAS
Clinical research
Regulatory knowledge
Data analysis
Cross-functional

Ausbildung

Master's degree
PhD

Tools

R
SAS

Jobbeschreibung

BD is seeking a Statistician/Biostatistician to support product development, clinical studies, and business decisions in a regulated healthcare environment. You will design studies, develop analysis plans, analyze data, and communicate insights to cross-functional teams.

The ideal candidate holds a Master’s or PhD in Statistics or Biostatistics with experience in clinical research or regulated medical devices. Proficiency in R and/or SAS and ability to manage multiple projects is essential.

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