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Expert Exploitation Specialist/Data Scientist

Culmen International LLC

Full-time | Contract

St. Louis, MO

Job description

Overview
Senior Statistical Sciences Programming Consultant will be responsible for statistical programming deliverables and will support real-world research projects and work on programming activities in post-market approval projects.

This position requires a comprehensive knowledge of SAS and CDISC standards, solid experience with real-world data (claims, EMR, registries) to inform reimbursement strategy and market access submissions.

Main Tasks

  • Provides statistical programming support to Medical Affairs research programs, publications, processing and applying real-world data, and other evidence generating activities.
  • Collaborates with counterparts in R&D Biostatistics, Clinical Data Management, Statistical Programming in providing support for a broad range of Medical Affairs programming activities.
  • Ensures efficiency and quality of deliverables of statistical analysis outputs.
  • Conduct statistical programming of clinical trial and real-world data using SAS and R Software.
  • Develops and QC statistical outputs.
  • Supports other departments for ad-hoc analyses and provide technical consulting on internal and external projects.

Qualifications:

  • Relevant academic degree either as a Bachelor of science with 12 years of pharma industry experience as a programmer or a Master of Science with 8 years of pharma industry experience as a programmer.
  • Knowledge of applying statistics and epidemiology on RWD. Familiarity with rare disease therapeutic and/or endocrinology areas is a plus.
  • Experienced in analyzing data from rare disease and/or product registry studies.
  • Experience in Medical Affairs statistical activities (e.g. RWE data generation, reimbursement filing, data mining, use of external data including historical control data, and real-world data).
  • Proficient in SAS with the ability to independently write code and provide guidance to other programmers for various activities and experience with developing code in R language.
  • Familiarity with regulatory guidelines for drug development. Experience in NDA/BLA/MAA submission is plus.
  • Proficient with CDISC standards.

Job Types: Full-time, Contract

Pay: From $100.00 per hour

Expected hours: 40 per week

Experience:

  • SAS programming: 8 years (Preferred)

Work Location: Remote