Clinical Research Coordinator I: Launch Your Trials Career

Velocity Clinical Research, Inc.; Texas; On-site; USD 42,000 - 64,000; Full time

Job summary

Velocity Clinical Research, Inc. is seeking a Clinical Research Coordinator I to conduct and manage clinical trials in accordance with study protocols, GCP, and Velocity SOPs.

You will coordinate startup activities, vendor management, subject recruitment, and regulatory submissions while maintaining high-quality data and patient safety. This role requires a Bachelor's degree with related experience (or equivalent) and strong knowledge of medical terminology, along with excellent communication

Qualifications

• Bachelor’s degree with 1 year of relevant experience in the life science industry or equivalent.
• Associate’s degree with 2 years of relevant experience in the life science industry or equivalent.
• High School graduate with minimum 3 years relevant experience in the life science industry.
• Phlebotomy and IM dose administration may be required by state law.

Responsibilities

• Conduct and manage clinical trials per protocol, GCP, and Velocity SOPs.
• Coordinate startup, vendor management, subject recruitment, scheduling, and regulatory documents.
• Enter data in sponsor/CRO data capture systems and resolve queries.
• Report adverse events and deviations; manage protocol amendments and close-out reports.
• Maintain confidentiality of patient, sponsor, and Velocity information.
• Ensure staff are trained, delegated appropriately, and compliant with guidelines.

Skills

Medical terminology

Microsoft Office

Communication skills

Team player

English proficiency

Multitasking

Detail oriented

Problem solving

Education

Bachelor’s degree in life sciences

Associate’s degree in life sciences

High School diploma or technical degree

Job description

Velocity Clinical Research, Inc. is seeking a Clinical Research Coordinator I to conduct and manage clinical trials in accordance with study protocols, GCP, and Velocity SOPs.

You will coordinate startup activities, vendor management, subject recruitment, and regulatory submissions while maintaining high-quality data and patient safety. This role requires a Bachelor's degree with related experience (or equivalent) and strong knowledge of medical terminology, along with excellent communication