Epidemiological Programmer Rwe, Fsp

IQVIA UK

Durham, United States
Base: $88,300.00 - $220,900.00; bonus/equity: ince...
Observational research using emr and claims data
Strong statistical programming skillset
Epidemiological study design
This Epidemiological Programmer role sits within our Real World Solutions team and will be responsible for leading development of datasets and conducting longitudinal analyses for observational studies in the virology therapeutic area under one client portfolio

Job Summary

  • This Epidemiological Programmer role sits within our Real World Solutions team and will be responsible for leading development of datasets and conducting longitudinal analyses for observational studies in the virology therapeutic area under one client portfolio.
  • In this role, individuals will have access to real-world databases and act as the stewards of the client’s best practices, standards, and methodologies underlying the use of real-world data (RWD).
  • IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries.

Matching Summary

This Epidemiological Programmer role sits within our Real World Solutions team and will be responsible for leading development of datasets and conducting longitudinal analyses for observational studies in the virology therapeutic area under one client portfolio.

Salary

Base: $88,300.00 - $220,900.00; Bonus/Equity: Incentive plans, bonuses may be offered; Benefits: Range of health and welfare and/or other benefits

Skills & Requirements

Must-have

  • observational research using EMR and claims data
  • strong statistical programming skillset
  • epidemiological study design
  • cohort building
  • RWE outcome measures
  • managing multiple studies and complex analyses
  • SAS and/or R, macros, SQL

Nice-to-have

  • applied proficiency in observational research
  • applied experience with epidemiological study design
  • applied proficiency of RWE study design
  • excellent analytic and communication skills
  • attention to detail

Key Requirements

  • Master's Degree with 5-8 years relevant experience or PhD with 3 years relevant experience
  • Strong track record of analysis of RWD
  • Demonstrated proficiency in advanced statistical programming
  • Demonstrated experience and applied proficiency of RWE study design
  • Prior pharmaceutical experience
  • Ability to effectively manage and prioritize multiple tasks

Work Rights

Not specified

Tailored Resume

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