Biostatistician, Clinical Trials & SAS

You will own and validate clinical trial data for YO AI Labs, a remote team supporting Sponsor and CRO workflows. In this contractor role, you will interpret SAPs, produce TFLs, and review CSRs while ensuring compliance with ICH E9(R1). You will collaborate with cross-functional teams to deliver accurate statistical outputs for regulatory submissions. This position offers a direct impact on trial integrity with a flexible remote schedule and a $60-$65/hour pay rate.

Own the statistical integrity of clinical trial data at YO AI Labs, a remote-first research organization. You will analyze and validate datasets, drive the delivery of Tables, Figures & Listings (TFLs), and ensure full compliance with regulatory standards like ICH E9(R1). Joining a lean team of biostatisticians and data scientists, you will collaborate directly with clinical and regulatory experts. This contract role offers the chance to shape submission-ready outputs across multiple therapeutic areas, with a focus on quality and precision.

At YO AI Labs, you will own the statistical integrity of clinical trial data across multiple remote projects. You will analyze datasets, validate outputs, and ensure regulatory compliance at the contract level. Your work directly supports sponsor and CRO teams, making SAS or R the core of your daily toolkit. This role stands apart through its focus on rigorous CDISC SDTM & ADaM standards and direct involvement in regulatory submissions.

You will own statistical analysis and validation for clinical trial data across multiple studies, directly supporting regulatory submissions. Your work ensures compliance and accuracy in all outputs. You will join a remote team of biostatisticians and data professionals, collaborating with cross-functional teams. This contract role offers $60–$65 per hour and the chance to impact drug development.

You will own statistical analysis and validation for clinical trial data, shaping studies from SAP to regulatory submission. You join a remote-friendly team supporting sponsors and CROs, using SAS and R to produce TFLs and review CSRs. Your work directly impacts drug development and regulatory approval, offering deep experience across therapeutic areas.

Biostatistician owns statistical analysis for clinical trial data, ensuring regulatory compliance and data integrity. You join a cross-functional team supporting sponsors and CROs remotely. This role stands out by offering direct involvement in regulatory submissions and quality control, with clear expectations for 5+ years of experience and expertise in SAS or R.