Principal R Programmer

IQVIA
Durham, NC, United States
2 days ago

Role details

Contract type
Permanent contract
Employment type
Full-time (> 32 hours)
Experience level
Expert
Experience required
5 years minimum
Compensation
$98,200.0 - $273,200.0
Working hours
Regular working hours

Tech stack

Data Analysis Clinical Data Management Computer Programming Data Cleansing Data Presentation Data Visualization R (Programming Language) Python (Programming Language) Markdown SAS (Software) Information Technology

Job description

Join a sponsor-dedicated team, progressing with in-house study activities over the years. Experienced R programmer needed to provide technical expertise for clinical PK/PD department to meet internal and external needs., * Data preparation and cleaning:

  • Cleaning and transforming raw clinical trial data from various sources to ensure accuracy and consistency for PK/PD analysis.
  • Programming PK/PD analyses:
  • Writing R or Rmarkdown code to perform descriptive analysis of PK/PD data and statistical analysis of exposure-response relationships.
  • Data visualization:
  • Creating clear and informative graphs and tables to effectively communicate PK/PD findings.
  • CDISC compliance:
  • Ensuring data is formatted according to CDISC standards for regulatory submissions
  • Validation and quality control:
  • Performing thorough validation checks on programming code and analysis results to maintain data integrity.
  • Identifies problems and develops tools that increase the efficiency and capacity of the Clinical PK/PD Programming group.

Requirements

  • Bachelor’s degree in Math, Stats, Computer Science or similar
  • 5+ years of industrial experience
  • Must have advanced R programming skills, including tidyverse, ggplot2, Markdown, Quarto, Shiny, etc. Python and/or SAS programming skills are a plus, but not required.
  • Knowledge of CDISC standards (SEND, SDTM, and ADaM) is required.
  • Desire to work in clinical PK/PD - knowledge and experience of PK/PD concepts and related programming is highly desirable.
  • Experience visualizing/presenting data for internal stakeholders or clients
  • Capable of implementing more advanced modeling and statistical procedures as requested by study team.
  • Strong understanding of clinical trial data and extremely hands on in data manipulations, analysis, and reporting/modeling of analysis results. Including handling of data issues and uncleaned data.
  • Professional attitude, self-motivated, logical thinking
  • Excellent attention to detail
  • Strong organization skills and ability to work on multiple tasks simultaneously while achieving quality standards and meeting deadlines
  • Good verbal and written communication skills. Strong interpersonal skills and ability to work collaboratively across teams
  • Ability to problem solve and develop innovative approaches along with a drive to learn and master new techniques and technologies

About the company

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at [click to reveal website link]https://jobs.iqvia.com

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