Clinical Research Assistant 2-Hematology

The Ohio State University Wexner Medical Center; Columbus (OH); On-site; USD 38,000 - 52,000; Full time

Job summary

The Ohio State University Wexner Medical Center in Columbus, OH seeks a Clinical Research Assistant to support PIs in the Hematology department. You will review medical records, assist with patient consent, data extraction, and longitudinal tracking of therapy, handling date entry and submission.

You will help with data quality control, monitor visits, resolve queries, screen participants, recruit, collect biospecimens, and prepare data for manuscripts and presentations.

Qualifications

• Bachelor’s Degree in Biological Sciences, Health Sciences or medical field; equivalent combination of education and experience.
• 0 years of relevant experience required.
• Background check and post-offer drug screen/physical may be required.

Responsibilities

• Review medical records and assist with patient consent.
• Extract data and track patients longitudinally through therapy; date entry and submission.
• Perform data quality control, schedule and conduct monitoring visits, and resolve queries.
• Screen participants, assist with recruitment and biospecimen collection.
• Compile and prepare research data for manuscripts and presentations.
• Communicate with other disciplines and collaborators to obtain quality data.
• Follow protocol design to ensure data elements are collected per guidelines and support quality assurance.
• Perform other duties as assigned by PIs and/or supervisor.

Skills

Data extraction

Consent support

Record review

Education

Bachelor's degree in Biological Sciences

Tools

EMR systems

Quality assurance tools

Job description

Scope/Summary

Clinical Research Assistant providing support to Principal Investigators (PIs) in the Department of Hematology; responsible for reviewing medical records, assisting with patient consent, and assisting with data extraction, tracking patients longitudinally through therapy, date entry and submission. Assisting with data quality control; scheduling and conducting monitoring visits and query resolution; participant screening, recruitment, and bio-specimen collection. Compiles and prepares research data results for manuscripts and presentations. Assists with communication with other disciplines and collaborators to obtain quality data for patients accrued to observational clinical research studies. Follows protocol design to ensure all appropriate data elements are collected in accordance with protocol guidelines. Responsible for internal and external quality assurance and quality reviews. Perform other duties as assigned by PIs and/or supervisor.

Minimum Required Qualifications

Bachelor’s Degree in Biological Sciences, Health Sciences or medical field, or equivalent combination of education experience required. 0 years of relevant experience required. 2-4 years of relevant experience preferred.

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

Thank you for your interest in working at Ohio State.

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