Senior Clinical Research Coordinator

Kaiser Permanente; San Diego (CA); On-site; USD 70,000 - 90,000; Full time

Job summary

Kaiser Permanente in San Diego seeks a clinical research associate to collect data for trials, prepare and submit study documentation to IRB/regulatory bodies, and support related lab operations. You will document activities with precision and assist with budget components across projects.

Responsibilities include developing compliant research materials, drafting trial applications, and ensuring confidentiality and data quality across sites.

Qualifications

• Bachelor's degree in Science, Public Health, Health Care Administration, or related field with 2 years of clinical research experience OR 5 years of clinical research experience.
• Certified Clinical Research Professional (CCRP) or related certification preferred.
• Basic Life Support (BLS) certification preferred.

Responsibilities

• Collects data for clinical trials and supports regulatory submissions with accuracy.
• Ensures compliance with federal, state, and local regulations and KP policies.
• Maintains and audits clinical research documentation and case files.
• Collaborates with cross-functional teams to support budgets and project timelines.

Skills

Ambiguity/Uncertainty Management

Attention to Detail

Communication

Critical Thinking

Cross-Group Collaboration

Decision Making

Dependability

Problem Solving

Teamwork

Learning Agility

Education

Bachelor's degree in Science / related field

Tools

Computer Literacy

Job description

Kaiser Permanente in San Diego seeks a clinical research associate to collect data for trials, prepare and submit study documentation to IRB/regulatory bodies, and support related lab operations. You will document activities with precision and assist with budget components across projects.

Responsibilities include developing compliant research materials, drafting trial applications, and ensuring confidentiality and data quality across sites.