Clinical Research Coordinator I — Fast-Paced Trials & Impact

Velocity-Clinical-Research,-Inc.; West of England; On-site; GBP 30,000 - 45,000; Full time

Job summary

Velocity Clinical Research seeks a Clinical Research Coordinator I to conduct and manage clinical trials in accordance with study protocol, GCP, and Velocity’s SOPs. The role requires coordinating startup activities, patient recruitment, visits, data entry, and QA of regulatory documents.

This position emphasizes careful documentation, timely reporting of adverse events, and collaboration with sponsors, CROs, and study teams in a fast paced environment.

Qualifications

• Bachelor’s degree with 1 year of relevant experience in life sciences OR
• Associate’s degree with 2 years of relevant experience in life sciences OR
• High School diploma with minimum 3 years relevant experience in life sciences

Responsibilities

• Conduct and manage clinical trials per protocol, GCP, and SOPs.
• Coordinate trials including startup, recruitment, visits, and data quality.
• Ensure adverse events are reported and regulatory documents are prepared.

Skills

Medical terminology

MS Office

Data entry

Team player

English proficiency

Communication skills

Documentation

Education

Bachelor’s degree in life sciences

Associate’s degree with relevant experience

High school + relevant experience

Tools

Computers

Microsoft Office

Fax

Copier

Multi-line telephone

Job description

Velocity Clinical Research seeks a Clinical Research Coordinator I to conduct and manage clinical trials in accordance with study protocol, GCP, and Velocity’s SOPs. The role requires coordinating startup activities, patient recruitment, visits, data entry, and QA of regulatory documents.

This position emphasizes careful documentation, timely reporting of adverse events, and collaboration with sponsors, CROs, and study teams in a fast paced environment.