Clinical Research Assistant 2-Hematology

The Ohio State University; North Carolina; On-site; USD 52,000 - 70,000; Full time

Job summary

The Ohio State University seeks a Clinical Research Assistant 2-Hematology to support PIs in the Hematology division. Responsibilities include reviewing medical records, assisting with patient consent, and data extraction, tracking patients through therapy, and data submission.

The role emphasizes data quality control, monitoring visits, query resolution, and coordination with other disciplines to obtain quality data for observational studies. Background checks may be required.

Qualifications

• Bachelor’s Degree in Biological Sciences, Health Sciences or medical field required.
• 0 years of relevant experience required; 2–4 years of relevant experience preferred.

Responsibilities

• Review medical records and assist with patient consent.
• Assist with data extraction, tracking patients longitudinally through therapy, data entry and submission.
• Assist with data quality control; schedule and conduct monitoring visits and query resolution.
• Participate in participant screening, recruitment, and bio-specimen collection.
• Prepare research data results for manuscripts and presentations; communicate with collaborators to ensure quality data.

Education

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

Job description

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Job Title

Clinical Research Assistant 2-Hematology

Department

Medicine | IM Hematology

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.

Location

Lincoln Tower (0271)

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.

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