Senior Research Nurse – Clinical Trials Specialist

Kaiser Permanente; Vallejo (CA); On-site; USD 110,000 - 140,000; Full time

Job summary

Kaiser Permanente in California seeks a Registered Nurse with clinical research experience to support protocol implementation, data collection, and regulatory compliance in clinical trials. The role emphasizes evidence-based practice, quality improvement, and collaboration with interdisciplinary teams to promote patient safety and research integrity.

Responsibilities include autonomous data collection, protocol development support, IRB submissions, and maintaining trial documentation while

Qualifications

• Bachelors degree in Nursing (or equivalent) and 2+ years of clinical health care experience.
• Associates degree in Nursing with 4+ years of clinical health care experience.
• California RN license required at hire.

Responsibilities

• Supports and collaborates with interdisciplinary teams to advance patient safety and clinical quality.
• Independently collects data in clinical trials and assists in protocol development and documentation.
• Adheres to regulatory requirements and prepares trial materials for IRB review.
• Maintains accurate documentation of research activities and findings.

Skills

Ambiguity/Uncertainty Management

Attention to Detail

Communication

Critical Thinking

Decision Making

Teamwork

Problem Solving

Learning Agility

Education

Bachelor's degree in Nursing

Associates degree in Nursing

Tools

Research Databases

Laboratory Equipment

Regulatory Knowledge

Project Management Tools

Job description

Kaiser Permanente in California seeks a Registered Nurse with clinical research experience to support protocol implementation, data collection, and regulatory compliance in clinical trials. The role emphasizes evidence-based practice, quality improvement, and collaboration with interdisciplinary teams to promote patient safety and research integrity.

Responsibilities include autonomous data collection, protocol development support, IRB submissions, and maintaining trial documentation while