Clinical Research Coordinator II - Data & Compliance

Kaiser Permanente; San Rafael (CA); On-site; USD 60,000 - 90,000; Full time

Job summary

Kaiser Permanente in San Rafael, CA is seeking a clinical research support role to collect trial data, prepare study documentation, and assist with regulatory submissions under guidance.

The position involves supporting budgeting for internal projects, ensuring compliance with federal, state, and local regulations, and contributing to the education of staff and participants on protocols and timelines.

Qualifications

• Bachelors degree or 3+ years in clinical research or related field.
• Experience with regulatory submissions and IRB processes is preferred.
• Knowledge of clinical research protocols and quality systems.

Responsibilities

• Collects data for clinical trials and supports study documentation.
• Assists with regulatory submissions and coordination with IRB.
• Supports budgeting input for internally funded projects.
• Maintains compliance with federally mandated protocols and KP policies.

Skills

Ambiguity management

Attention to detail

Communication

Critical thinking

Teamwork

Problem solving

Learning agility

Organizational skills

Data quality

Compliance

Stakeholder management

Education

Bachelor's degree in Science, Public Health, Health Care Administration, or a directly related field

CCRP/ACRP/HCCA certifications (preferred)

Tools

Laboratory Equipment

Laboratory Procedures

Computer Literacy

Job description

Kaiser Permanente in San Rafael, CA is seeking a clinical research support role to collect trial data, prepare study documentation, and assist with regulatory submissions under guidance.

The position involves supporting budgeting for internal projects, ensuring compliance with federal, state, and local regulations, and contributing to the education of staff and participants on protocols and timelines.