Clinical Research Coordinator II - Lead Trials & Data

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

401k with match

Annual incentive

Job summary

Velocity Clinical Research is seeking a Clinical Research Coordinator II to manage multiple trials from start-up to close-out, ensuring GCP compliance and high data quality. The role involves coordinating start-up activities, subject recruitment, scheduling visits, and maintaining regulatory documentation.

The candidate will monitor adverse events, ensure timely data entry, and collaborate with the team to implement QC measures and improve study outcomes.

Qualifications

• Bachelor’s degree with 2+ years life science experience OR
• Associate’s degree with 4+ years life science experience OR
• High School/technical with 6+ years life science experience and 1 year CRC experience

Responsibilities

• Conduct and manage clinical trials per protocol, GCP, and SOPs.
• Coordinate start-up, recruitment, visits, data entry, and regulatory documents.
• Manage adverse events reporting and protocol amendments.
• Collaborate to develop QC strategies and ensure timely data queries resolution.

Skills

Medical terminology

MS Office

Communication

Teamwork

Attention to detail

English fluency

Education

Bachelor’s degree + 2 years life sciences

Associate’s degree + 4 years life sciences

High school diploma + 6 years life sciences

Tools

None

Job description

Velocity Clinical Research is seeking a Clinical Research Coordinator II to manage multiple trials from start-up to close-out, ensuring GCP compliance and high data quality. The role involves coordinating start-up activities, subject recruitment, scheduling visits, and maintaining regulatory documentation.

The candidate will monitor adverse events, ensure timely data entry, and collaborate with the team to implement QC measures and improve study outcomes.