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Biostatistician I (part-time) at Jobgether. This position is posted by Jobgether on behalf of a partner company. We are currently looking for a . Biostatistician I. in . Colorado (USA). .. This part-time role is an excellent opportunity for an early-career biostatistician seeking to apply statistical expertise to clinical research and trials. You will work closely with project teams to design studies, analyze data, and ensure high-quality statistical support across a range of therapeutic areas. The position involves active collaboration with colleagues, programming in SAS, and contributing to meaningful clinical outcomes. You will also gain exposure to regulatory environments and professional development opportunities while maintaining a flexible work schedule.. . Accountabilities. In this role, you will:. . Support study design, statistical analysis, and communication of findings to project teams.. . Provide regular progress updates and seek guidance from senior biostatisticians when needed.. . Review and validate electronic data capture designs and assist with edit check development.. . Apply statistical methods appropriately to study designs and analyses.. . Use SAS for programming, validation, analysis, and reporting of clinical data.. . Prepare documentation, statistical programs, and reports for interim and final analyses.. . Collaborate with team members to resolve programming or analytical issues.. . Contribute to manuscripts, abstracts, grants, and sponsor requests when required.. . Ensure compliance with SOPs, regulatory guidelines, and industry standards.. . Engage in professional development through conferences, journals, or associations.. . . To be successful in this position, you should bring:. . Master’s degree in biostatistics or a related field, with at least 1 year of clinical trial analysis experience.. . Demonstrated programming proficiency with SAS (version 9.0 or higher).. . Familiarity with Microsoft Office tools (Word, Excel, PowerPoint).. . Knowledge of ICH guidelines, Phase I–III trials, CDISC standards, and FDA/NDA submissions.. . Strong analytical, organizational, and communication skills with excellent attention to detail.. . Ability to interpret study protocols and statistical analysis plans effectively.. . Capacity to work on multiple trials or tasks simultaneously in a fast-paced environment.. . Note: Applicants must successfully pass a background and education verification check.. . Company Location: United States.