Clinical Research Specialist II - Data Abstraction

Kaiser Permanente; Pasadena (CA); On-site; USD 65,000 - 90,000; Full time

Job summary

KAISER in Pasadena, California, is seeking a Clinical Research Specialist II to support data collection and chart abstraction. The role involves executing day-to-day project operations, assisting with recruitment, consent, and participant follow-up, and ensuring adherence to GCP and IRB protocols.

You will help develop study materials, manage documentation, and coordinate with investigators and project managers.

Qualifications

• Bachelor's degree in Public Health, Health Care Administration, Epidemiology, Health Sciences, Social or Behavioral Sciences, Health Services, Statistics, or Health Economics, or related field.
• OR Minimum three (3) years of experience in health research, public health, laboratory or social science research setting, epidemiology, social or behavioral sciences, health services or a directly related field.

Responsibilities

• Assist with day-to-day operations of research projects and ensure regulatory compliance.
• Support recruitment, enrollment, consenting, and follow-up with participants.
• Draft study materials in various formats including online.
• Document and report study activities using project tracking tools.
• Coordinate supplies, meetings, and IRB-related documentation and approvals.
• Conduct literature reviews to support grant proposals and IRB protocol amendments.

Skills

Ambiguity/Uncertainty Management

Attention to Detail

Communication

Critical Thinking

Teamwork

Problem Solving

Learning Agility

Organizational Savvy

Stakeholder Management

Health Care Industry

Education

Bachelor's degree in Public Health or related field

Job description

KAISER in Pasadena, California, is seeking a Clinical Research Specialist II to support data collection and chart abstraction. The role involves executing day-to-day project operations, assisting with recruitment, consent, and participant follow-up, and ensuring adherence to GCP and IRB protocols.

You will help develop study materials, manage documentation, and coordinate with investigators and project managers.