Clinical Research Coordinator I - Fast-Paced Trials

Velocity Clinical Research, Inc.; Austin (TX); On-site; USD 52,000 - 76,000; 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 support start-up activities, patient recruitment, data collection, and regulatory documentation to ensure high-quality data and patient safety. Ideal candidates have a life science background and the ability to work in a fast-paced environment, with strong communication and organizational skills, and willingness

Qualifications

• Bachelor’s degree with 1 year of relevant life science experience, or associate’s with 2 years, or high school with 3 years.
• Phlebotomy and IM dose administration may be required by state law.
• Demonstrated knowledge of medical terminology.
• Proficient in basic computer/office tools and ability to work in a fast-paced environment.
• Ability to read, write and speak English; strong communication and organizational skills.
• Willingness to travel locally and nationally.

Responsibilities

• Conduct and manage clinical trials per protocol and GCP.
• Coordinate start-up, vendor management, recruitment, data entry, and regulatory documents.
• Ensure timely data entry and resolve queries; report adverse events.
• Communicate professionally with study teams, sponsors, CROs, and vendors.
• Create, collect, and submit regulatory documents to Sponsors and IRBs.
• Promote confidentiality and patient safety.

Skills

Medical terminology

Fast-paced environment

Communication skills

Interpersonal skills

Team player

English proficiency

Multitasking

Problem solving

Professionalism

Detail oriented

Education

Bachelor's degree in life sciences

Associate's degree in life sciences

High school diploma with relevant experience

Tools

Microsoft Office

Computers

Fax machine

Copier

Multi-line telephone

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 support start-up activities, patient recruitment, data collection, and regulatory documentation to ensure high-quality data and patient safety. Ideal candidates have a life science background and the ability to work in a fast-paced environment, with strong communication and organizational skills, and willingness