Data Management Specialist

The Ohio State University, Main Campus

. Support management, quality control, analysis, and reporting of clinical research data for the Center for Tobacco Research .

Posted 9/17/2026full-timeColumbus • Ohio • United StatesMid-LevelSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical research data management, statistical analysis, and reporting, with proficiency in REDCap and data integration from multiple sources. Strong ability to maintain data quality, collaborate with multidisciplinary teams, and prepare comprehensive research reports and visualizations.

Highest-signal resume keywords

REDCap Database ManagementStatistical AnalysisData Quality AssuranceStatistical Software (SAS, R)Clinical Research Methodology

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Statistical AnalysisData ManagementData CleaningData IntegrationStatistical ReportingData VisualizationQuality ControlDataset PreparationRecruitment Metrics MonitoringHuman-Subjects Research Compliance

Soft Skills

Attention to DetailOrganizational SkillsWritten CommunicationVerbal CommunicationTeam Collaboration

Tools & Technologies

REDCapSASRStatistical Software

Industry Keywords

Clinical ResearchBiostatisticsEpidemiologyData ScienceHuman-Subjects Research

About the role

Key responsibilities & impact

Support management, quality control, analysis, and reporting of clinical research data for the Center for Tobacco Research
Monitor and manage study data, including recruitment and retention metrics, data quality, databases, data integration, statistical analyses, and reports
Assist with management and maintenance of clinical research databases in REDCap
Perform routine data-quality checks and resolve discrepancies with clinical research staff
Clean, organize, and prepare datasets for statistical analysis and reporting
Assist with database closeout and preparation of final analysis datasets
Integrate data from multiple sources with primary REDCap databases
Document data-management procedures, quality-control processes, and dataset modifications
Compile and disseminate weekly and monthly study reports
Prepare reports on recruitment, enrollment, retention, study progress, and performance metrics
Conduct routine statistical analyses under Senior Biostatistician supervision
Prepare statistical tables, figures, summaries, visualizations, presentations, abstracts, and manuscript materials
Support clinical studies through participant recruitment, screening, scheduling, visits, data collection, specimen collection, and study procedures
Enter and verify participant data in REDCap and other study systems
Maintain compliance with institutional policies, study protocols, and human-subject research requirements
Collaborate with biostatisticians, research coordinators, research nurses, investigators, and Center personnel
Participate in study meetings and develop increasing independence in data management, statistical programming, and research reporting

Requirements

What you’ll need

Bachelor's Degree in Management Information Systems, Health Sciences, Computer Science or relevant field
Demonstrated knowledge of fundamental statistical concepts and methods
Experience working with statistical or data-management software
Strong attention to detail and ability to identify errors, inconsistencies, and data-quality issues
Ability to organize and manage multiple projects and priorities in a clinical research environment
Strong written and verbal communication skills
Ability to work effectively independently and as part of a multidisciplinary research team
Final candidates must successfully complete a background check
A drug screen or physical may be required during the post-offer process
Preferred: Master's degree in biostatistics, statistics, epidemiology, data science, or closely related field
Preferred: Experience with SAS and/or R
Preferred: Experience with REDCap or other clinical research database systems
Preferred: Experience managing, cleaning, or integrating research datasets from multiple sources
Preferred: Experience preparing statistical tables, figures, or research reports
Preferred: Familiarity with clinical research methodology and human-subjects research
Preferred: Experience with longitudinal, clinical, behavioral, or pharmacokinetic data
Preferred: Experience supporting scientific manuscripts, abstracts, presentations, or publications
Preferred: Experience with data visualization and presentation of research findings
Preferred: Previous experience in a clinical research or academic research environment

Benefits

Comp & perks

Regular position with 40 scheduled hours per week
First shift schedule
Hybrid work arrangement
Professional development and mentorship under the Senior Biostatistician
Equal opportunity employment, including veterans and disability