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10 дней назад

Senior Epidemiological Programmer, Real World Evidence - FSP

88 300 - 220 900$
Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
Вакансия из списка Hirify.GlobalВакансия из Hirify Global, списка международных tech-компаний
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Описание вакансии

Текст:
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TL;DR
Senior Epidemiological Programmer, Real World Evidence - FSP (SAS/R, SQL, Virology): Developing analytic datasets and conducting longitudinal analyses for observational virology studies using claims, EHR, and laboratory data with an accent on cohort building, epidemiological study design, and advanced statistical programming. Focus on handling censored and missing data, confounding, survival analysis, regression models, propensity score methods, and QC of TFLs.

Location: Durham, North Carolina, United States of America

Salary: $88,300–$220,900 annualized base pay

Company

IQVIA provides clinical research services, commercial insights, and healthcare intelligence for the life sciences and healthcare industries.

What you will do

  • Lead development, processing, cleaning, and quality control of analytic datasets from claims, EHR, EMR, and laboratory data, including Optum, HealthVerity, TriNetX, and IQVIA PharMetrics Plus.
  • Assess the feasibility of real-world data sources, characterize patient populations, build cohorts, and define and validate study variables.
  • Conduct and QC analyses using diagnosis and treatment codes and statistical methods for censored data, confounding, differing person-time, and missing data.
  • Collaborate with epidemiologists on study design, methodology, statistical specifications, and complex longitudinal, survival, regression, and propensity score analyses for virology research.
  • Develop and QC tables, figures, and listings for protocols, reports, and manuscripts, and support protocols, statistical analysis plans, and study reports.
  • Communicate timelines, progress, and results while providing technical, programming, statistical, and epidemiological solutions for complex studies.

Requirements

  • Master’s degree in Biostatistics, Epidemiology, Outcomes Research, or a related field with 5–8 years of relevant experience, or a PhD with 3 years of relevant experience.
  • Strong track record analyzing real-world data using EMR and claims data.
  • Advanced statistical programming proficiency using SAS and/or R, macros, and SQL.
  • Applied proficiency in real-world evidence study design, terminology, cohort building, and analytic methodologies.
  • Prior pharmaceutical or CRO experience.
  • Excellent analytical and communication skills with attention to detail.
  • Ability to manage and prioritize multiple tasks and projects effectively.

Culture & Benefits

  • Work within the environment of a prominent pharmaceutical company as part of a dedicated Real World Evidence FSP team.
  • Access real-world databases and steward client best practices, standards, and methodologies for real-world data.
  • Base pay varies according to qualifications, education, experience, location, and schedule.
  • Incentive plans, bonuses, health and welfare benefits, and other benefits may be offered depending on the position.
  • Equal opportunity employment is provided.

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