Clinical Research Coordinator-Hematology

Ohio State University; North Carolina; On-site; USD 55,000 - 75,000; Full time

Job summary

Ohio State University in Lincoln Tower is seeking a Clinical Research Coordinator-Hematology to oversee observational hematology protocols. You will screen patients, obtain informed consent, coordinate visits, monitor data quality, and support regulatory submissions while collaborating with the Division of Hematology and the OSUWMC team.

The role requires a Bachelor's in Biological/Health/Social Sciences or related field and 1 year of clinical research experience; 2–4 years preferred.

Qualifications

• 1 year of relevant clinical research experience required.
• 2-4 years of relevant experience preferred.

Responsibilities

• Coordinate and oversee clinical research protocols in hematology observational studies.
• Identify and assess patient eligibility for participation.
• Obtain informed consent and discuss studies with patients and families.
• Assist with data quality control, data extraction, and report generation.
• Support IRB submissions, amendments, and regulatory compliance.
• Schedule and monitor visits and ensure data integrity and reporting.

Skills

Clinical research

IRB familiarity

Education

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

Job description

Job Title: Clinical Research Coordinator-Hematology

Department: Medicine | IM Hematology

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.

Additional Information

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.

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