Hematology Clinical Research Coordinator — Patient Data

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

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.