Clinical Research Assistant 2-Hematology

The Ohio State University Wexner Medical Center; Columbus (OH); On-site; USD 42,000 - 56,000; Full time

Job summary

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

You will aid with data quality control, scheduling monitoring visits, participant screening and bio-specimen collection, and preparation of results for manuscripts.

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.

Responsibilities

• Review medical records for study eligibility and data elements.
• Assist with patient consent and enrollment activities.
• Aid in data extraction and longitudinal tracking of therapy.
• Support data quality control and query resolution.
• Schedule and conduct monitoring visits.
• Screen participants, recruit, and collect biospecimens as needed.
• Compile research results for manuscripts and presentations.
• Communicate with collaborators to ensure data quality.
• Follow protocol design to ensure complete data collection.
• Assist with internal and external quality assurance; perform other duties as assigned by PIs.

Education

Bachelor’s Degree in Biological Sciences, Health Sciences or medical field

Job description

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