Associate Clinical Data Analyst / Programmer

About CG Oncology, Inc.

Are you ready to make a difference in the world and become part of our patient-centered team that is focused on Attacking Bladder Cancer for a Better Tomorrow? At CG Oncology, we believe that by having exceptionally talented individuals on our team who share our passion and enjoy working together, we can truly achieve our Vision and Mission to benefit patients around the world.

Every day we are making significant advancements across our multiple pipelines and are growing rapidly to meet the needs of our patients who cannot afford to wait to benefit from our novel immunotherapies. Please review this job posting and our Values and if they resonate with you and are what you expect from your organization and team, then we would like to hear from you.

About the role

At CG Oncology, clinical data drives critical decisions that shape how new oncology therapies are developed. In this role, you’ll work hands-on with real clinical trial data—building datasets, analyses, and reports that directly support study execution and internal decision-making.

This opportunity is ideal for an early-career clinical data professional who wants to grow technical depth in clinical programming while learning how high-quality data enables successful clinical development in a regulated biotech environment.

Location: Remote

Essential Functions

• Over your first year, you’ll progressively take ownership of core clinical data deliverables, including:
• Build and deliver validated clinical analysis datasets (SDTM, ADaM) from raw data in compliance with CDISC, GxP, and ICH standards.
• Develop and maintain SAS and SQL programs to generate datasets, tables, listings, figures, and recurring reports that withstand validation and review.
• Support fit-for-purpose clinical analyses used in internal data reviews and decision-making.
• Create dashboards and visualizations that help teams track study progress, data quality, and key metrics.
• Collaborate cross-functionally with Clinical Operations, Data Management, Biostatistics, and Clinical Science to clarify requirements and deliver accurate, timely outputs.
• Grow technical independence by writing clean, maintainable code, troubleshooting issues, and improving processes over time.

You’re successful in this role if:

• Your datasets and outputs consistently pass review with minimal rework
• Your code is clear, well-documented, and reusable
• You proactively identify data issues and help resolve them
• You steadily increase ownership and confidence in your programming and analysis work
• Stakeholders trust the accuracy and clarity of the data you deliver

Qualifications

• Have 1–2+ years of experience in biotech, pharma, or a CRO
• Enjoy working with clinical trial data and care deeply about data quality
• Have hands-on experience or training in SAS, SQL, and CDISC standards (SDTM, ADaM)
• Are curious, detail-oriented, and eager to learn in a regulated environment
• Communicate clearly and collaborate well with cross-functional partners

Education: Bachelor’s or Master’s degree in Statistics, Data Science, Computer Science, Bioinformatics, or a related field (or equivalent experience).

We hire for long-term success. This role is designed to be a true growth opportunity, where your development and CG Oncology’s clinical goals advance together.

Please note that CG Oncology does not accept unsolicited information and/or resumes from search firms or agencies for our job postings. Any resumes or client information submitted to our careers page or any employee of CG Oncology by any search firm or agency without an applicable contract in place will become the property of CG Oncology and no fee(s) will be paid.

Total Rewards

CG Oncology offers very competitive and comprehensive Total Rewards, helping to support and reward our