Senior Epidemiological Programmer, Real World Evidence - FSP
Контакты
88 300 - 220 900$
Формат работы
onsite
Тип работы
fulltime
Грейд
senior
Английский
b2
Страна
US
sqlrsasepidemiologyvirologystatistical programmingreal world evidencesurvival analysispropensity score methods
Вакансия из Hirify Global, списка международных tech-компаний Для мэтча и отклика нужен Plus
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Зарплата и рынок
Мало
$88к-221к/год
$140к$160кмедиана$200к
По похожим ролям (49) ~ $160к/год
На СНГ рынке: $4.2к/мес ($3.6к - $4.4к)
69
Хорошая вакансия
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Обязанности четко описаны и дают узкую экспертизу в RWE, но зарплата ниже рыночного ориентира, а широкий диапазон не позволяет понять вероятный уровень предложения.
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Ниже рынкаШирокий диапазонАктуальный стекЧеткие задачиЭкспертиза в RWE
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Описание вакансии
Текст:
Hirify AI/Оригинал
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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