What are the responsibilities and job description for the Clinical Research Assistant-Hematology position at The Ohio State University Wexner Medical Center?
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Clinical Research Assistant providing support to Principal Investigators (PIs) in the Department of Hematology; responsible for reviewing medical records and assisting with data extraction, tracking of 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 an/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.
Screen reader users may encounter difficulty with the online application. For assistance with applying, please contact hr-accessibleapplication@osu.edu. If you have questions while submitting an application, please review these frequently asked questions.
Thank you for your interest in working at Ohio State.
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.
Clinical Research Assistant providing support to Principal Investigators (PIs) in the Department of Hematology; responsible for reviewing medical records and assisting with data extraction, tracking of 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 an/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.
Screen reader users may encounter difficulty with the online application. For assistance with applying, please contact hr-accessibleapplication@osu.edu. If you have questions while submitting an application, please review these frequently asked questions.
Thank you for your interest in working at Ohio State.
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.