Clinical Trials Coordinator II — Study Delivery & Data

Velocity-Clinical-Research,-Inc.; Florida; On-site; USD 60,000 - 80,000; 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 seeks a Clinical Research Coordinator II to conduct and manage multiple trials from start-up through close-out in line with the study protocol, GCP, and Velocity SOPs.

Responsibilities include coordinating start-up, vendor management, subject recruitment, data entry, safety reporting, and regulatory submissions while maintaining confidentiality and high-quality data.

Qualifications

• Bachelor's degree and 2 years relevant experience in life sciences OR
• Associate's degree with 4 years relevant experience in life sciences OR
• High School/technical degree with minimum 6 years relevant experience in life sciences AND 1 year Clinical Research Coordinator experience

Responsibilities

• Conduct and manage multiple clinical trials from start up through close out.
• Ensure adherence to study protocol, GCP, and SOPs.
• Coordinate start up, vendor management, recruitment, data entry, and regulatory documents.
• Monitor safety reporting and regulatory compliance.
• Communicate effectively with sponsors, CROs, and team members.

Skills

Medical terminology

Microsoft Office

Fast-paced environment

Verbal communication

Written communication

Organizational skills

Team player

English proficiency

Detail oriented

Problem solving

Leadership

Education

Bachelor's degree

Associate's degree

High School diploma/technical degree

Job description

Velocity Clinical Research seeks a Clinical Research Coordinator II to conduct and manage multiple trials from start-up through close-out in line with the study protocol, GCP, and Velocity SOPs.

Responsibilities include coordinating start-up, vendor management, subject recruitment, data entry, safety reporting, and regulatory submissions while maintaining confidentiality and high-quality data.