Clinical Research Coordinator II: Fast-Paced Trials & Data

Velocity Clinical Research, Inc.; San Mateo (CA); On-site; USD 85,962,000 - 103,155,000; Full time

Benefits offered by this job

Medical insurance

Dental insurance

Vision insurance

Paid time off

401(k) with company-match

Annual incentive program

Job summary

Velocity Clinical Research, Inc. seeks a dedicated professional to conduct and manage clinical trials in accordance with study protocols, GCP, ICH guidelines and Velocity SOPs. You will coordinate startup activities, vendor management, subject recruitment, data capture and adverse event reporting.

Join a team focused on high-quality data, patient safety, and rapid study execution while maintaining strict regulatory standards and effective collaboration with sponsors, CROs, and sites.

Qualifications

• Bachelor's degree or higher with related life science experience.
• Experience handling clinical trial documentation and regulatory requirements.
• Strong written and verbal communication skills.

Responsibilities

• Conduct and manage clinical trials per study protocol, GCP, ICH and SOPs.
• Coordinate startup, vendor management, recruitment, data entry and QA processes.
• Manage adverse events reporting and regulatory submissions.
• Collaborate with team to ensure timely, compliant trial conduct.

Skills

Medical terminology

MS Office

Fast-paced environment

Verbal communication

Interpersonal skills

Team player

English fluency

Multi-tasking

Attention to detail

Problem solving

Leadership

Education

Bachelor's degree in life sciences

Associate's degree with 4 years relevant experience

High School diploma with 6 years relevant experience

Job description

Velocity Clinical Research, Inc. seeks a dedicated professional to conduct and manage clinical trials in accordance with study protocols, GCP, ICH guidelines and Velocity SOPs. You will coordinate startup activities, vendor management, subject recruitment, data capture and adverse event reporting.

Join a team focused on high-quality data, patient safety, and rapid study execution while maintaining strict regulatory standards and effective collaboration with sponsors, CROs, and sites.