Clinical Research Coordinator II, Contract

Job Description

Job Description

Salary : $38 - $44 per hour

Clinical Research Coordinator II - Vaccine Trials, Independent Contractor

Company : Kinetic Clinical Research

Location : Long Beach, CA

Employment Type : Independent Contractor (1-month temporary assignment)

Schedule : 6 days / week, assigned shift : 7 : 00AM - 3 : 00PM OR 12 : 00PM - 8 : 00PM

Hourly Rate : $38.00 - $44.00 / hour

About Us

Kinetic Clinical Research operates a network of clinical trial sites across Southern California, serving diverse patient populations through community-focused care. We deliver high-performance results while maintaining strict ethical and regulatory standards.

The Role

We need an experienced Clinical Research Coordinator II with vaccine trial expertise for an urgent 1-month contract assignment at our Long Beach site. You'll provide critical coordination support for multiple high-volume vaccine studies during peak enrollment, working within our established team to manage complex vaccination protocols and safety monitoring procedures.

What You'll Do

• Coordinate vaccine trial protocols for Phase I-IV preventive and therapeutic vaccine studies
• Screen, enroll, and schedule participants according to vaccine-specific inclusion / exclusion criteria
• Coordinate vaccine administration visits and post-vaccination safety assessments
• Monitor participants for adverse reactions and manage follow-up safety evaluations
• Support vaccine storage, handling, and accountability documentation
• Maintain vaccination records, adverse events, and safety data with precision
• Coordinate specimen collection for immunogenicity assessments and safety laboratories
• Schedule follow-up visits and safety phone calls per protocol requirements
• Support regulatory documentation and vaccine accountability records
• Assist with preparation for sponsor monitoring visits and regulatory inspections

What We're Looking For

Required :

Preferred :

Why Join Us

How to Apply

Submit your resume emphasizing your vaccine clinical trial experience, immunization administration background, and high-volume study coordination capabilities. Include specific examples of vaccine adverse event management and safety monitoring experience. Immediate start required.

Kinetic Clinical Research is an Equal Opportunity Employer committed to workplace diversity. We do not discriminate on the basis of race, color, religion, gender, sexual orientation, gender identity, national origin, age, disability, veteran status, or any other protected status under federal, state, or local law.