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Sr. R Programmer (Pk/Pd)

Propharma
Propharma
3+ years
Not Disclosed
Remote, USA, Remote
10 May 6, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Company Overview

ProPharma Group has over 20 years of experience improving patient health and wellness by supporting biotech, medical device, and pharmaceutical organizations.

Through its advise–build–operate model, ProPharma delivers end-to-end solutions across the product lifecycle, with expertise in:

  • Regulatory Sciences

  • Clinical Research Solutions

  • Quality & Compliance

  • Pharmacovigilance

  • Medical Information

  • R&D Technology


Role Title

Clinical PK/PD Programmer (R Programming) (Title inferred based on responsibilities)


Role Summary

This role focuses on developing custom programming solutions using R and companion tools to support clinical pharmacokinetic/pharmacodynamic (PK/PD) analysis.

The position involves:

  • Data preparation and analysis

  • Statistical programming

  • Data visualization

  • Ensuring regulatory compliance and data quality


Key Responsibilities

1. Data Preparation & Cleaning

  • Clean and transform raw clinical trial data from multiple sources

  • Ensure data accuracy, consistency, and readiness for PK/PD analysis


2. PK/PD Programming & Analysis

  • Develop R/RMarkdown code to:

    • Perform descriptive PK/PD analyses

    • Conduct exposure-response statistical analysis

  • Generate:

    • Summary tables

    • Data listings

    • Graphs

    • Derived datasets


3. Data Visualization

  • Create clear and insightful:

    • Graphs

    • Tables

  • Effectively communicate findings to stakeholders


4. CDISC Compliance

  • Ensure datasets comply with:

    • SEND

    • SDTM

    • ADaM standards

  • Support regulatory submission readiness


5. Validation & Quality Control

  • Perform validation checks on:

    • Programming code

    • Analysis outputs

  • Maintain data integrity and quality standards


6. Process Improvement

  • Identify inefficiencies in workflows

  • Develop tools and solutions to improve team efficiency and capacity


Education Requirements

  • Bachelor’s degree in:

    • Mathematics

    • Statistics

    • Computer Science

    • Or a related field


Experience Requirements

  • Minimum 3+ years of industry experience

  • Hands-on experience with:

    • Clinical trial data

    • Data manipulation, analysis, and reporting

  • Preferred:

    • PK/PD domain knowledge

    • Experience with advanced statistical modeling


Technical Skills

  • Advanced proficiency in:

    • R programming, including:

      • tidyverse

      • ggplot2

      • RMarkdown / Quarto

      • Shiny

  • Additional (optional):

    • Python

    • SAS

  • Strong understanding of:

    • CDISC standards (SEND, SDTM, ADaM)


Core Competencies

  • Strong analytical and problem-solving skills

  • High attention to detail and data accuracy

  • Excellent organizational and multitasking abilities

  • Ability to meet deadlines while maintaining quality

  • Strong communication and interpersonal skills

  • Ability to work collaboratively across teams

  • Self-motivated with a proactive, learning-oriented mindset


Work Environment

  • Remote work supported

  • Hybrid work encouraged for employees near office locations


Work Culture & Values

  • Commitment to Diversity, Equity & Inclusion

  • Equal Opportunity Employer

  • Encourages innovation, collaboration, and authenticity

  • Supportive and inclusive workplace environment


Application Process

  • Applications are personally reviewed by the recruitment team

  • No AI-based screening tools are used

  • All applicants receive a response


Important Notice

  • No unsolicited resumes from recruiters or third parties

  • No phone calls or emails regarding this role