Research Assistant

The Ohio State University, Main Campus

Student Research Associate coordinating clinical research and participant safety in Dr. Keller-Hamilton’s lab.

Posted 8/5/2026part-timeColumbus • Ohio • 🇺🇸 United StatesEntry LevelWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in coordinating clinical research activities, ensuring compliance with GCP, IRB, and FDA regulations, while effectively managing participant recruitment and data integrity throughout the study lifecycle.

Highest-signal resume keywords

Clinical Research CoordinationGCP ComplianceIRB Submission PreparationData Quality ChecksParticipant Recruitment

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Data EntryElectronic Data CaptureRegulatory Binder MaintenanceStudy Protocol AdherenceAdverse Event Documentation

Soft Skills

Organizational SkillsAttention to DetailWritten CommunicationVerbal Communication

Industry Keywords

Clinical StudiesParticipant SafetyOperational ChallengesAudit-Ready DocumentationStudy Progress Updates

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Support the coordination and execution of clinical research activities within Dr. Brittney Keller-Hamilton’s lab
Support day-to-day activities of clinical studies
Assist with participant recruitment, screening, enrollment, and retention efforts
Coordinate study visits and ensure adherence to protocol schedules
Maintain study timelines and identify and address operational challenges
Assist with preparation and submission of IRB applications, amendments, continuing reviews, and study reports
Maintain current, audit-ready regulatory binders
Support internal and external audits and monitoring visits
Collect, enter, and verify study data in electronic data capture systems
Perform data quality checks and resolve queries
Maintain accurate source documentation, study databases, and tracking logs
Liaise between investigators, participants, and study team members
Participate in team meetings and provide study progress updates
Monitor participant safety and adverse events
Document and report adverse events and protocol deviations
Provide education and support to study participants throughout the trial

Requirements

What you’ll need

Pursuing a bachelor’s degree in public health or related field
Strong organizational skills and attention to detail
Excellent written and verbal communication skills
Compliance with GCP, IRB requirements, FDA regulations, institutional policies, and study protocols
Successful completion of a background check
A drug screen or physical may be required during the post-offer process

Benefits

Comp & perks

Medical, dental and vision coverage, with Ohio State paying a significant portion of the cost
Paid time off, including sick and vacation time and 11 holidays
State retirement plan or an alternative retirement plan, both with generous employer contributions
Growth opportunities
Access to boundless resources
Strong sense of community and commitment to excellence