R Programmer

Are you an experienced R Programmer with a profound passion for clinical research and data analysis? Aegists is actively seeking a talented and dedicated R Programmer to join our innovative team, providing essential clinical programming support to our esteemed Pharma/Biotech clients across the US. This crucial role offers a unique opportunity to apply your robust R programming expertise in a highly critical and impactful field, contributing directly to significant advancements in global healthcare. We are looking for a meticulously detail-oriented professional who not only excels in complex data manipulation and sophisticated data visualization but also deeply understands and skillfully implements industry-standard methodologies to ensure data integrity and reliable analytical outcomes. As an R Programmer at Aegists, you will be at the forefront of transforming raw clinical data into actionable insights, playing a pivotal role in the lifecycle of clinical trials.

Key Responsibilities

• Develop, validate, and meticulously execute R programs for comprehensive clinical trial data analysis, ensuring accuracy and reproducibility.
• Perform advanced statistical programming to generate high-quality Tables, Listings, and Figures (TLFs) critical for regulatory submissions and scientific publications.
• Ensure strict adherence to clinical data standards, particularly CDISC, including the creation and validation of SDTM and ADaM datasets.
• Collaborate effectively with cross-functional teams, including biostatisticians, data managers, and clinical scientists, to interpret study protocols and deliver precise, timely programming outputs.
• Contribute significantly to the development, review, and maintenance of programming documentation, standard operating procedures (SOPs), and programming specifications.
• Conduct rigorous data quality checks and efficiently resolve any programming-related discrepancies or issues to maintain data integrity.
• Actively participate in the review of study protocols, statistical analysis plans, and other critical study documents to provide programming input and ensure feasibility.
• Develop reusable R functions and macros to improve efficiency and consistency in programming tasks across multiple projects.

Requirements

• Demonstrated strong professional programming experience with R, specifically within a clinical research or pharmaceutical environment.
• Proven proficiency in clinical trial data programming, including expertise in handling complex and varied datasets.
• In-depth familiarity and practical application of CDISC standards, encompassing SDTM and ADaM dataset creation and validation.
• Proven ability to generate publication-quality Tables, Listings, and Figures (TLFs) using R, suitable for regulatory submissions and internal reports.
• Exceptional analytical skills complemented by extensive experience in data analysis and advanced visualization techniques using R packages (e.g., ggplot2, plotly).
• Comprehensive understanding of the clinical research process, drug development lifecycle, and relevant regulatory guidelines (e.g., FDA, ICH).
• Strong problem-solving abilities, meticulous attention to detail, and a commitment to producing high-quality, reproducible work.
• Excellent communication skills, both written and verbal, for effective collaboration with diverse scientific and non-scientific teams.

What We Offer

• The unique opportunity to engage with and support leading Pharma/Biotech clients on groundbreaking and impactful clinical development projects.
• A highly collaborative, inclusive, and supportive work environment that fosters innovation and professional growth.
• Direct exposure to cutting-edge clinical research methodologies and advanced data science techniques.
• Dedicated opportunities for continuous professional development, training, and career advancement within a specialized domain.
• A competitive compensation package reflecting your experience and contributions to our success and the value you bring to our clients.

If you are a highly motivated R Programmer eager to make a tangible difference in patient outcomes and thrive in a challenging yet rewarding environment, we encourage you to apply. Join Aegists and leverage your expertise to contribute to critical pharmaceutical advancements. We value innovation, precision, and a commitment to scientific excellence in all our team members.