Statistician

• Department of Orthopaedic Surgery and Sports Medicine University of Florida
• 4.2 Gainesville, FL Job Details Full-time $61,000
• $70,000 a year 21 hours ago Qualifications Data integrity assurance Bioinformatics Statistics Bayesian inference Data visualization software proficiency Clinical study protocols and reports Statistics Biostatistics-based research Medical statistical report preparation Bachelor's degree in statistics Data validation techniques Medical software

SAS R HIPAA FDA 21 CFR

Part 11 Mid-level Reporting and dashboarding tools SAS language Research project design Master's degree GDPR compliance expertise Data integrity and documentation Analysis skills ICH guidelines Statistics research Bachelor's degree Data quality monitoring Clinical program data analysis

Mentoring Full Job Description JOB NO:

540605

WORK TYPE:

Staff Full-Time

LOCATION

Main Campus (Gainesville, FL)

CATEGORIES

Health Care Administration/Support

DEPARTMENT

29170000

• MD-ORTHOPAEDICS
• REHAB

CLASSIFICATION TITLE

Data Scientist

I CLASSIFICATION MINIMUM REQUIREMENTS 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.

JOB DESCRIPTION

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 include:

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.

EXPECTED SALARY

$61,000

• $70,000; commensurate with education and experience.

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.

PREFERRED

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 a meticulous approach to data handling and documentation.

Preferred Skills :

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.

SPECIAL INSTRUCTIONS TO APPLICANTS

In order to be considered, you must upload your cover letter and resume. Application must be submitted by 11:55 p.m. (ET) of the posting end date.

HEALTH ASSESSMENT REQUIRED

No

ADVERTISED

15 Jul 2026 Eastern Daylight Time

APPLICATIONS CLOSE

29 Jul 2026 Eastern Daylight Time