On-Site Cardiovascular Clinical Research Coordinator

The Ohio State University; Columbus (OH); On-site; USD 45,000 - 70,000; Full time

Job summary

The Ohio State University invites applications for a Clinical Research Coordinator in Cardiovascular Medicine within the Department of Internal Medicine. This on-site position coordinates daily clinical research activities, recruits and consents patients, and ensures regulatory compliance.

Responsibilities include data collection and analysis, scheduling, patient follow-up, adverse event monitoring, and preparation for IRB and sponsor reviews.

Qualifications

• Bachelor’s Degree in Biological Sciences, Health Sciences, Social Sciences or other medical field, or equivalent combination of education/experience.
• 1 year of relevant experience required.
• Background check (and possibly pre-employment physical/drug screen) may be required.

Responsibilities

• Coordinate and perform daily clinical research activities per approved protocols.
• Recruit, interview and enroll patients; obtain informed consent.
• Coordinate scheduling and follow-through of patient care appointments and procedures.
• Assist with data collection, data extraction, coding and analysis of clinical data.
• Monitor patients for adverse reactions and notify appropriate clinical staff and sponsors.
• Ensure compliance with IRB, FDA and sponsor regulations; participate in external quality reviews.
• Contribute to development of new protocols and study goals.

Skills

Medical terminology

Microsoft Office

Regulatory knowledge

Education

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

Tools

REDCap

Job description

The Ohio State University invites applications for a Clinical Research Coordinator in Cardiovascular Medicine within the Department of Internal Medicine. This on-site position coordinates daily clinical research activities, recruits and consents patients, and ensures regulatory compliance.

Responsibilities include data collection and analysis, scheduling, patient follow-up, adverse event monitoring, and preparation for IRB and sponsor reviews.