Clinical Research Assistant 2-Hematology

Wexner Medical Center; Columbus (OH); On-site; USD 42,000 - 62,000; Full time

Job summary

Wexner Medical Center seeks a Clinical Research Assistant to support Principal Investigators in the Hematology department. You will review medical records, assist with patient consent, and help extract data while tracking patients longitudinally through therapy and data entry.

You will oversee data quality control, schedule monitoring visits, resolve queries, screen participants and collect bio-specimens. You will prepare data for manuscripts and presentations and coordinate with collaborators

Qualifications

• Bachelor’s Degree in Biological Sciences, Health Sciences or related field.
• 0 years of relevant experience required; 2–4 years preferred.
• Background check and possible drug screen may be required post offer.

Responsibilities

• Review medical records and assist with patient consent.
• Assist with data extraction and longitudinal tracking of patients.
• Support PIs with data quality control and monitoring visits; resolve queries.
• Prepare data for manuscripts and presentations.
• Coordinate communication with collaborators to obtain quality data.

Skills

Medical record review

Data extraction

Quality control

Study coordination

Communication with collaborators

Education

Bachelor's degree in Biological Sciences/Health Sciences or related field

Job description

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.