Clinical Research Assistant 2- Cancer Awards

Job Title:

Clinical Research Assistant 2
- Cancer

Awards Department: CCC | Cancer Awards

The Clinical Research Associate (CRA) will support the coordination and execution of clinical research activities within Dr. Brittney Keller-Hamilton's lab. This role is responsible for ensuring studies are conducted in compliance with regulatory requirements, institutional policies, and study protocols while maintaining high-quality data and participant safety. The CRA will work collaboratively with investigators, study coordinators, regulatory teams, and external partners to support study operations across the lifecycle of clinical trials.

• Study Coordination & Operations:
  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 proactively identify and address operational challenges.
• Regulatory Compliance:
  Ensure compliance with GCP, IRB requirements, FDA regulations, and institutional policies;
  Assist with preparation and submission of IRB applications, amendments, continuing reviews, and study reports;
  Maintain regulatory binders (electronic and/or paper) ensuring documents are current and audit-ready;
  Support internal and external audits and monitoring visits.
• Data Management & Quality:
  Collect, enter, and verify study data in electronic data capture (EDC) systems;
  Perform routine data quality checks and resolve queries in a timely manner;
  Ensure accurate and complete source documentation;
  Assist in maintaining study databases and tracking logs.
• Collaboration & Communication:
  Serve as a liaison between investigators, participants, and study team members;
  Participate in team meetings and provide updates on study progress.
• Participant Safety &
  
  Experience:
  
  Ensure participant safety through adherence to protocol and monitoring for adverse events;
  Document and report adverse events and protocol deviations per guidelines;
  Provide education and support to study participants throughout the trial.

• Bachelor's degree in public health or related field
• Strong organizational skills and attention to detail
• Excellent written and verbal communication skills

Location:

Olentangy River Rd, 3650 (2520)

Position Type:
Regular

Scheduled

Hours:

40

Shift: First Shift

Final candidates are subject to successful completion of a background check. A drug screen or physical may be required during the post offer process.

• 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.

The university is an equal opportunity employer, including veterans and disability.

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