Clinical Research Coordinator-Hematology

Wexner Medical Center; Columbus (OH); On-site; USD 52,000 - 76,000; Full time

Job summary

Wexner Medical Center seeks a Clinical Research Coordinator to coordinate hematology malignancy studies, focusing on observational protocols and patient eligibility assessments.

You will obtain informed consent, assist with data quality control, and support IRB submissions, monitoring, and QA. Collaboration across divisions and external sponsors is required, with data extraction and reporting responsibilities.

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.

Responsibilities

• Coordinate and oversee clinical research protocols in hematology malignancies, including eligibility assessment and patient discussions.
• Obtain informed consent and assist with data quality control and query resolution.
• Schedule and conduct monitoring visits; assist with IRB submissions and amendments.

Skills

Clinical research coordination

Informed consent process

Data management

Regulatory compliance

IRB submissions

Education

Bachelor’s degree in Biological Sciences/Health Sciences/Social Sciences or related 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.