Data Analyst & Research Compliance Specialist

University of South Florida•Tampa, FL

About The Position

We are seeking a highly organized, detail-oriented professional to serve in dual roles as an Institutional Review Board (IRB) Specialist and Statistical Analyst. This unique role supports compliance with research ethics and regulatory requirements while providing advanced statistical expertise for data analysis and reporting. This position will work directly with the Assistant Dean for Medical Student Research and the research team on day-to-day activities, including, but not limited to, IRB protocol submission support and coordination, data management, statistical analysis, and research dissemination. The incumbent ensures compliance with human subjects’ research regulations, manages datasets, performs complex analyses, and assists with manuscripts and grant proposals. The role also includes training new staff, maintaining quality assurance programs, and serving as a resource for faculty, medical students, and team members. This position is not eligible for Visa Sponsorship.

Requirements

Bachelor’s degree in Biostatistics, Epidemiology, Mathematics, Public Health, or a related field and at least two years of research experience; OR Master’s degree in one of the same fields with a minimum of one year of research experience.

Nice To Haves

Master’s degree with three years of research experience, or Doctoral degree (PhD, DrPH) with at least one year of research experience.
Certification in IRB administration (e.g., CIP).
Experience with clinical, observational research, meta-analysis, and systematic reviews.
Proficiency in multiple statistical software packages and data visualization tools.
Strong scientific writing and communication skills.

Responsibilities

Maintain regular contact with the USF IRB office to understand the protocol submission-related processes and guidelines, etc.
Serve as a guide for medical students, residents, and fellows for IRB protocol design and submission, amendments, renewals, closing out the studies, etc.
Ensure compliance with federal regulations, institutional policies, and ethical standards.
Serve as a liaison between investigators and the IRB, guiding protocol development and informed consent, etc.
Maintain accurate records of IRB approvals and correspondence.
Monitor ongoing studies for adherence to approved protocols and reporting requirements.
Develop and maintain data sets, ensuring data integrity and quality.
Collaborate with investigators to design studies, calculate sample sizes, and select appropriate statistical tests.
Perform statistical analyses using appropriate methodologies (e.g., propensity score matching, multivariate regression, survival analysis, etc.).
Assist in interpreting results and drafting methods/results sections for peer-reviewed manuscripts.
Prepare statistical reports, tables, and visualizations for peer-reviewed manuscripts and presentations.