Clinical Research Coordinator-Hematology

The Ohio State University Wexner Medical Center; Columbus (OH); On-site; USD 50,000 - 65,000; Full time

Job summary

The Ohio State University Wexner Medical Center is seeking a Clinical Research Coordinator to oversee hematology malignancy studies, primarily observational. You will identify eligible patients, discuss studies with patients and families, and assist with informed consent and data quality control.

You will coordinate IRB submissions, collaborate with a multidisciplinary team, and help prepare reports and grant-related documents while ensuring regulatory compliance and data integrity.

Qualifications

• Bachelor's degree in a biological/health field required or equivalent.
• 1 year of relevant clinical research experience required; 2-4 years preferred.
• Experience coordinating research activities and ensuring data integrity preferred.

Responsibilities

• Coordinate and oversee clinical research protocols in hematology malignancies.
• Identify and assess eligibility of patients for participation in studies.
• Discuss studies with patients and families and obtain informed consent.

Skills

Clinical Research Coordination

Patient recruitment

Data quality control

IRB submissions

Education

Bachelor's degree in Biological Sciences, Health Sciences, Social Sciences or other medical field

Job description

Clinical Research Coordinator responsible for the coordination and oversight of clinical research protocols investigating hematology malignancies primarily in observational studies, within the Division of Hematology; coordinates clinical research activities to include identifying and assessing eligibility of patients for clinical research study participation; discussing research studies with patients and their family members; obtains informed consent, assists with data quality control; scheduling and conducting monitoring visits and query resolution; participant screening, recruitment, and bio-specimen collection. Assists with IRB submissions, modifications and amendments; collaborates with an interdisciplinary research team made up of members from the Division of Hematology, other personnel within the OSUWMC, as well as external; ensures that all necessary data is collected and reported as appropriate; provides support to the members of the clinical research team in developing plans to meet the requirements of new clinical research studies; participates in writing manuscripts and in preparation of grant submissions; researches, develops and creates detailed reports and presentations in response to data and reporting requests; participates in internal and external quality reviews; analyzes, queries, interprets and summarizes data; collects and extracts data; ensures and verifies data integrity. Generates reports and reviews to ensure validity of data; supports activities to ensure compliance with all Institutional Review Boards (IRB), FDA (Federal Drug Administration), federal, state and industry sponsor regulations; assists with coordinating and preparing for external quality assurance and control reviews by IRB, federal or industry sponsors.

Minimum Required Qualifications

Bachelor's Degree in Biological Sciences, Health Sciences, Social Sciences or other medical field, or equivalent combination of education experience required. 1 year of relevant clinical research experience required. 2-4 years of relevant experience preferred.

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.