Clinical Research Coordinator - RN II

Lancesoft INC; California; On-site; USD 72,000 - 103,000; Full time

Job summary

LanceSoft is seeking a Clinical Research Coordinator – RN II in Newport Beach, CA to manage and coordinate complex clinical trials across phases I–IV. The role requires collaboration with physicians, sponsors, and research teams to ensure compliance with GCP, FDA regulations, and human subject protection standards.

Salary is $52–$75 per hour, with a full-time, onsite schedule, Mon–Fri 8:30 AM–5:00 PM. Preferred qualifications include a BSN, IATA certification, and IRB documentation experience.

Qualifications

• 2+ years of clinical research experience or equivalent training
• Active RN license – California
• BLS Certification
• Knowledge of Good Clinical Practices (GCP), FDA regulations, and human subject protection
• Strong organizational, analytical, and communication skills
• Proficiency in Microsoft Word, PowerPoint, and Windows applications
• Ability to work in a fast-paced research environment

Responsibilities

• Manage and coordinate complex clinical research trials including industry-sponsored, government-funded, and investigator-initiated studies.
• Conduct protocol review and study preparation prior to trial initiation.
• Manage the informed consent process according to regulatory standards.
• Recruit, screen, and assess study participants based on eligibility criteria.
• Collect and process laboratory samples in compliance with IATA standards.

Skills

Clinical research

RN license

GCP knowledge

FDA regulations

Regulatory compliance

Microsoft Office

Fast-paced environment

Education

BSN (preferred)

Job description

Job Description

Clinical Research Coordinator – RN II

Location: Newport Beach, CA
Salary: $52 – $75 per hour Based on the years of experience
Job Type: Direct Hire | Full-Time | Onsite
Position Overview:

We are seeking a Clinical Research Coordinator – RN II to manage and coordinate complex clinical research trials including drug, device, and biologic studies across Phase I–IV trials. This role works closely with physicians, sponsors, and research teams to ensure compliance with Good Clinical Practice (GCP), FDA regulations, and human subject protection standards.

Schedule: Full-Time Mon – Fri 8:30 AM – 5:00 PM

Key Responsibilities:

• Manage and coordinate complex clinical research trials including industry-sponsored, government-funded, and investigator-initiated studies.
• Conduct protocol review and study preparation prior to trial initiation.
• Manage the informed consent process according to regulatory standards.
• Recruit, screen, and assess study participants based on eligibility criteria.
• Collect and process laboratory samples in compliance with IATA standards.

Required Qualifications:

• 2+ years of clinical research experience or equivalent training
• Active Registered Nurse (RN) license – California
• Basic Life Support (BLS) Certification
• Knowledge of Good Clinical Practices (GCP), FDA regulations, and human subject protection
• Strong organizational, analytical, and communication skills
• Proficiency in Microsoft Word, PowerPoint, and Windows applications
• Ability to work in a fast-paced research environment

Preferred Qualifications:

• Bachelor of Science in Nursing (BSN)
• Knowledge of FDA, NIH, and OHRP regulatory requirements
• Experience with Institutional Review Board (IRB) documentation
• Understanding of clinical trial methodologies
• ACRP or SoCRA certification
• IATA certification

Company Description

LanceSoft is rated as one of the largest staffing firms in the US by SIA. Our mission is to establish global cross-culture human connections that further the careers of our employees and strengthen the businesses of our clients. We are driven to use the power of our global network to connect businesses with the right people, and people with the right businesses without bias. We provide Global Workforce Solutions with a human touch.