Clinical Research Coordinator I - Fast-Paced Trials

Velocity Clinical Research, Inc.; Cincinnati (OH); On-site; USD 42,000 - 65,000; Full time

Benefits offered by this job

Medical, dental, and vision insurance

Paid time off and company holidays

401(k) retirement plan with company‑匹h

Annual incentive program

Job summary

Velocity Clinical Research, Inc. seeks a Clinical Research Coordinator I to conduct and manage trials per protocol, GCP, and Velocity SOPs. You will coordinate startup activities, vendor management, recruitment, logging regulatory documents, and monitoring data entry.

The role emphasizes timely data entry, query resolution, patient safety, and collaboration with sponsors, CROs, and team members while upholding confidentiality. Strong English communication and attention to detail are essential.

Qualifications

• Bachelor’s or equivalent with life science experience.
• Strong knowledge of medical terminology and data entry.
• Proficient in MS Office and professional communication.

Responsibilities

• Conduct and manage trials per protocol, GCP, and SOPs.
• Coordinate startup, vendor management, recruitment, and visits.
• Ensure data entry timely and resolve data queries.
• Maintain confidential information and report adverse events.

Skills

Medical terminology

Data entry

Microsoft Office

English communication

Team collaboration

Attention to detail

Education

Bachelor’s degree with 1 year of life science experience

Associate’s degree with 2 years of life science experience

High School Diploma or technical degree with 3 years life science experience

Tools

Computers

Fax

Copier

Phone system

Job description

Velocity Clinical Research, Inc. seeks a Clinical Research Coordinator I to conduct and manage trials per protocol, GCP, and Velocity SOPs. You will coordinate startup activities, vendor management, recruitment, logging regulatory documents, and monitoring data entry.

The role emphasizes timely data entry, query resolution, patient safety, and collaboration with sponsors, CROs, and team members while upholding confidentiality. Strong English communication and attention to detail are essential.