Principal R Programmer Consultant

November 17

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ClinChoice

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Biotechnology • Pharmaceuticals • Healthcare Insurance

ClinChoice is a global full-service contract research organization (CRO) established in 1995, specializing in clinical development, post-marketing, and functional service support for the pharmaceutical, biotechnology, and medical devices industries. They provide comprehensive solutions from early clinical development to post-approval lifecycle management, with expertise in a variety of therapeutic areas such as autoimmune and inflammation, dermatology, endocrinology, infectious diseases, neuroscience, and oncology. ClinChoice aims to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. The company supports its clients with clinical, regulatory, and operational expertise across all phases of product development.

1001 - 5000 employees

Founded 1998

🧬 Biotechnology

💊 Pharmaceuticals

⚕️ Healthcare Insurance

📋 Description

• Develop, validate, and maintain analysis datasets (SDTM/ADaM), Tables, Listings, and Figures (TLFs) in support of clinical trial reporting using SAS and R. • Design and implement data visualization dashboards in Power BI to support clinical development teams, safety monitoring, and cross-functional data reviews. • Collaborate closely with biostatistics, data management, clinical operations, and other functional teams to ensure accurate, timely, and efficient programming deliverables. • Contribute to the development, refinement, and documentation of standard macros, templates, and programming processes. • Participate in the review of study protocols, CRFs, and statistical analysis plans (SAPs) to ensure alignment with data reporting and visualization strategies. • Ensure compliance with CDISC standards (SDTM, ADaM) and applicable regulatory requirements (e.g., FDA, EMA). • Provide technical mentorship and support to junior programmers and contribute to training initiatives. • Lead or contribute to programming activities in support of regulatory submissions (e.g., define.xml, reviewer guides, data packages).

🎯 Requirements

• Bachelor’s or Master’s degree in Computer Science, Statistics, Life Sciences, or related field. • 5+ years of experience in clinical programming within pharmaceutical, biotech, or CRO environments. • Expert-level programming skills in SAS (Base, Macro, SQL) and strong experience with R (including packages like tidyverse, haven, ggplot2). • Proficiency in developing dashboards and reports using Power BI (including DAX and Power Query). • Solid knowledge of CDISC SDTM and ADaM standards and experience applying them in clinical trials. • Familiarity with regulatory submission requirements and documentation for FDA/EMA. • Strong analytical, problem-solving, and organizational skills. • Ability to manage multiple priorities and work collaboratively across cross-functional teams.

🏖️ Benefits

• Health insurance • Professional development opportunities