Clinical Research Coordinator II: Drive Clinical Trials

Velocity Clinical Research, Inc.; Cincinnati (OH); On-site; USD 55,000 - 75,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

Paid time off

Company holidays

401(k) with company-match

Annual incentive program

Job summary

Velocity Clinical Research, Inc. is seeking a Clinical Research Coordinator II to oversee multiple trials from initiation to close-out in accordance with study protocols, GCP, and Velocity SOPs.

Responsibilities include start-up coordination, subject recruitment, data management, and safety reporting. The role requires strong medical terminology knowledge, proficiency in Microsoft Office, and excellent communication skills, with emphasis on teamwork and adherence to regulatory requirements.

Qualifications

• Bachelor’s degree and 2 years relevant life science experience OR
• Associate’s degree with 4 years life science experience OR
• High school or technical degree with minimum 6 years life science experience AND 1 year CRC experience

Responsibilities

• Conduct and manage clinical trials from start-up to close-out per study protocol and GCP
• Coordinate start-up, vendor management, recruitment, data entry and query resolution
• Manage adverse events and protocol amendments, prepare close-out reports
• Communicate with sponsors, CROs, vendors and team; maintain confidentiality

Skills

Medical terminology

Microsoft Office

Verbal communication

Team player

English proficiency

Education

Bachelor’s degree + 2 years life science

Associate’s degree + 4 years life science

High school + 6 years life science + 1 year CRC experience

Tools

None

Job description

Velocity Clinical Research, Inc. is seeking a Clinical Research Coordinator II to oversee multiple trials from initiation to close-out in accordance with study protocols, GCP, and Velocity SOPs.

Responsibilities include start-up coordination, subject recruitment, data management, and safety reporting. The role requires strong medical terminology knowledge, proficiency in Microsoft Office, and excellent communication skills, with emphasis on teamwork and adherence to regulatory requirements.