Clinical Research Coordinator II: Trials Lead & Data

Velocity Clinical Research, Inc.; St. Louis (MO); On-site; USD 52,000 - 76,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

Paid time off

401(k) retirement plan with company-m

Annual incentive program

Job summary

Velocity Clinical Research, Inc. in St. Louis, MO seeks a Clinical Research Coordinator II to manage multiple trials from start-up through close-out in line with protocol and GCP.

You will coordinate startup, vendor management, subject recruitment, data collection and regulatory documentation, while ensuring QA, safety reporting, and timely data entry.

Join a team focused on delivering high-quality data and exemplary patient care in a fast-paced environment.

Qualifications

• Bachelor’s degree with 2 years relevant life science experience OR
• Associate’s degree with 4 years relevant life science experience OR
• High School Diploma with 6 years life science experience AND 1 year Clinical Research Coordinator experience

Responsibilities

• Conduct and manage clinical trials in line with protocol, GCP, ICH and Velocity SOPs.
• Coordinate startup, vendor management, subject recruitment and data collection.
• Apply project management concepts to manage risk and improve quality of conduct.
• Develop and implement strategies to manage assigned protocols.
• Communicate professionally with coworkers, sponsors, CROs and vendors.
• Ensure confidential handling of patient data and sponsor information.

Skills

Medical terminology

Communication skills

Team player

English proficiency

Multi-tasking

Detail oriented

Education

Bachelor’s degree (life science)

Associate’s degree (life science)

High school diploma with 6 years life science experience

Tools

Microsoft Office

Fax

Copier

Multi-line telephone

Job description

Velocity Clinical Research, Inc. in St. Louis, MO seeks a Clinical Research Coordinator II to manage multiple trials from start-up through close-out in line with protocol and GCP.

You will coordinate startup, vendor management, subject recruitment, data collection and regulatory documentation, while ensuring QA, safety reporting, and timely data entry.

Join a team focused on delivering high-quality data and exemplary patient care in a fast-paced environment.