Principal R Programmer
ProPharma - Raleigh, North Carolina, United States, 27601
Work at ProPharma
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Overview
Principal R Programmer
role at
ProPharma . ProPharma has spent the past 20 years improving patient health and wellness by providing expert advice and solutions that empower biotech, med device, and pharmaceutical organizations to advance scientific breakthroughs and develop new therapies. The company partners with clients through an advise-build-operate model across the entire product lifecycle, leveraging deep expertise in regulatory sciences, clinical research, quality & compliance, pharmacovigilance, medical information, and R&D technology. ProPharma offers a comprehensive suite of customizable consulting solutions to de-risk and accelerate high-profile drug and device programs. The role involves using R and companion software to develop custom code for generating summary tables, data listings, graphs, and derived datasets according to the statistical analysis plan and programming specifications. Ensuring outputs meet quality standards and project requirements is essential. Essential Functions
Data preparation and cleaning: transforming raw clinical trial data from various sources for accuracy and consistency in PK/PD analysis. Programming PK/PD analyses: writing R or Rmarkdown code for descriptive and statistical analysis of PK/PD data. Data visualization: creating graphs and tables to communicate PK/PD findings effectively. CDISC compliance: formatting data according to CDISC standards for regulatory submissions. Validation and quality control: performing validation checks on code and results to maintain data integrity. Problem-solving: developing tools to increase the efficiency and capacity of the Clinical PK/PD Programming group. Training: providing training to fellow programmers on industry guidelines and software features relevant to the role. Minimum Requirements
Bachelors degree in Math, Stats, Computer Science, or similar. 7+ years of industrial experience. Advanced R programming skills, including tidyverse, ggplot2, Markdown, Quarto, Shiny, etc. Knowledge of Python and/or SAS is a plus. Knowledge of CDISC standards (SEND, SDTM, ADaM). Interest or experience in clinical PK/PD concepts and programming. Experience visualizing and presenting data to stakeholders. Ability to implement advanced modeling and statistical procedures. Strong understanding of clinical trial data, data manipulation, analysis, and reporting. Professional attitude, self-motivated, logical thinker. Attention to detail, organizational skills, multitasking ability. Excellent communication skills, collaborative mindset. Problem-solving skills and eagerness to learn new techniques. ProPharma values diversity and inclusion, creating a workplace where everyone can be their authentic self. We are committed to equity and provide a safe space for all employees to succeed. ***ProPharma Group does not accept unsolicited resumes from recruiters or third parties. Please, no phone calls or emails regarding this posting.*** Additional Details
Seniority level: Mid-Senior level Employment type: Full-time Job function: Engineering and Information Technology Industries: Business Consulting and Services
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