Clinical Research Operations Specialist

Kaiser Permanente

Pasadena (CA)

Hybride

USD 55 000 - 85 000

Plein temps

14 jours+

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Résumé du poste

Kaiser Permanente in Pasadena, CA seeks a Research Support role to execute day-to-day project operations, support research studies, and ensure compliance with IRB protocols. You will contribute to data collection, recruitment, consent, and participant follow-up, while helping draft study materials and maintain documentation.

Responsibilities include data validation, literature reviews, and assisting senior staff with study documentation, IRB amendments, and regulatory adherence in a fast-paced

Qualifications

  • Bachelor's degree in Public Health, Health Care Administration, Epidemiology, Health Sciences, Social/Behavioral Sciences, Health Services, Statistics, or Health Economics, or related field.
  • Or Minimum three (3) years of experience in health research or related field.

Responsabilités

  • Supports day-to-day research project operations and data collection.
  • Assists with recruitment, enrollment, consent, and follow-up with participants.
  • Prepares study materials and documentation; maintains study files and records.
  • Maintains compliance with IRB protocols and regulatory requirements.

Connaissances

Attention to Detail
Communication
Cross-Group Collaboration
Decision Making
Problem Solving
Teamwork
Learning Agility
Integrity
Adaptability
Responsibility

Formation

Bachelor's degree in Public Health
Or 3+ years health research experience

Outils

Good Clinical Practices (GCP)
IRB Procedures

Description du poste

Kaiser Permanente in Pasadena, CA seeks a Research Support role to execute day-to-day project operations, support research studies, and ensure compliance with IRB protocols. You will contribute to data collection, recruitment, consent, and participant follow-up, while helping draft study materials and maintain documentation.

Responsibilities include data validation, literature reviews, and assisting senior staff with study documentation, IRB amendments, and regulatory adherence in a fast-paced

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