Statistician - Department of Orthopaedic Surgery and Sports Medicine
Listed on 2026-07-20
-
IT/Tech
Data Scientist, Data Analyst
Overview
Statistician - Department of Orthopaedic Surgery and Sports Medicine
Location:
Main Campus (Gainesville, FL)
• Full Time
The Statistician applies rigorous statistical methodologies to design, analyze, and interpret clinical research studies. The role supports investigators in planning trials, monitoring data integrity, and creating reports that meet regulatory standards. The role blends technical expertise with collaboration across multidisciplinary teams to ensure data integrity, accessibility, and security.
Responsibilities- Design study protocols, randomization schemes, sample size calculations, and interim analysis plans.
- Develop and validate statistical analysis plans (SAPs) that align with regulatory guidelines (e.g., FDA, EMA) and internal standards.
- Conduct statistical analyses on clinical trial data, ensuring accuracy, reproducibility, and compliance with pre‑specified methods.
- Collaborate with biostatisticians, data managers, and clinical teams to address data‑quality issues and troubleshoot analyses.
- Prepare and review statistical sections of study reports, manuscripts, and regulatory submissions.
- Participate in protocol development meetings, providing statistical input on feasibility, outcomes, and endpoints.
- Mentor junior staff and trainees in statistical concepts and best practices.
- Develop and supervise data collection, entry, and validation protocols for clinical and research studies.
- Maintain and optimize electronic data capture (EDC) platforms (e.g., REDCap, EPIC, custom solutions).
- Implement data quality assurance processes, including audits, error tracking, and query resolution.
- Ensure compliance with institutional, federal, and state regulations (IRB, HIPAA, GDPR, etc.).
- Produce routine data summaries, statistical reports, and dashboards for investigators, clinicians, and administrators.
Occasional travel to study sites, conferences, or regulatory meetings may be required.
Qualifications- A Bachelor's Degree in data science, statistics, bioinformatics, analytics, or similar field and two years of experience;
Master’s Degree in data science, statistics, bioinformatics, analytics, or similar field.
Expected Salary: $61,000 - $70,000; commensurate with education and experience.
Preferred Qualifications- Proficiency in statistical software (e.g., SAS, R, SPSS) and experience with clinical trial data systems.
- Solid understanding of regulatory requirements (ICH GCP, FDA 21 CFR Part 11, EMA guidelines).
- Strong analytical skills and meticulous data handling and documentation.
- Experience with adaptive designs, Bayesian methods, or advanced longitudinal modeling.
- Familiarity with data visualization tools and effective communication of complex results to non‑statistical audiences.
- Ability to work collaboratively in multidisciplinary teams and manage multiple projects concurrently.
- Critical‑thinking mindset with a proactive approach to problem solving.
To be considered, upload your cover letter and resume. Applications must be submitted by 11:55 p.m. (ET) of the posting end date.
Health and ComplianceHealth Assessment
Required:
No
Applications Close: 29 July 2026
the UF Jobs site: explore.jobs.ufl.edu/en-us/job/540605
Our CommitmentThe University of Florida is an Equal Employment Opportunity Employer. Hiring is contingent on eligibility to work in the U.S. The University of Florida is a public institution and is subject to all requirements under Florida Sunshine and Public Record laws. If an accommodation due to a disability is needed to apply for this position, please call or the Florida Relay System at (TDD) or visit Accessibility at UF.
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