Clinical Research Associate II - Protocol & Study Lead

aa067

Duarte (CA)

On-site

USD 70,000 - 90,000

Full time

3 days ago
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Job summary

City of Hope in Duarte, CA seeks a Clinical Research Associate II to manage multiple research protocols, ensuring regulatory compliance and efficient study conduct. You will work with investigators, coordinate patient registration, data collection, and adherence to study timelines.

The role supports protocol-related tests and evaluations, contributes to recruitment efforts, and mentors junior staff. A clinical research background and at least an associate’s degree are required, with preference

Qualifications

  • Associate’s degree required; experience may substitute for education requirements.
  • One year of experience in a health care setting, preferably in research.
  • Minimum of 6 months CRA I experience at City of Hope.

Responsibilities

  • Conduct protocol management for multiple research protocols.
  • Maintain protocol documentation and notify investigators of changes.
  • Ensure patient registration and maintain registration documentation.
  • Compile and submit data on forms according to protocol requirements.
  • Monitor protocol compliance and schedule protocol-related tests.
  • Participate in patient recruitment to studies.
  • Train and mentor new clinical research staff.
  • Collect and deliver specimens using required equipment.
  • Coordinate tests and evaluations with physicians or nurses as per protocol.

Skills

Protocol management
Regulatory compliance
Data collection
Patient recruitment
Staff training

Education

Associate’s degree
Bachelor's degree

Job description

City of Hope in Duarte, CA seeks a Clinical Research Associate II to manage multiple research protocols, ensuring regulatory compliance and efficient study conduct. You will work with investigators, coordinate patient registration, data collection, and adherence to study timelines.

The role supports protocol-related tests and evaluations, contributes to recruitment efforts, and mentors junior staff. A clinical research background and at least an associate’s degree are required, with preference

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