Geriatrics Assistant Clinical Research Coordinator - 50% Limited

UCLA Health

Los Angeles (CA)

On-site

USD 37,000 - 60,000

Full time

2 days ago
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Job summary

UCLA Health in Los Angeles, CA is seeking an Assistant Clinical Research Coordinator to support day-to-day operations of clinical research studies and work closely with coordinators to ensure successful study implementation. The role involves study coordination, data collection, and administrative tasks while maintaining compliance with protocols and regulatory requirements.

This position is described as a limited role that may convert to a career, with an hourly salary reflecting market rates

Responsibilities

  • Support the implementation and coordination of one or more clinical research studies.
  • Assist with participant recruitment, study visits, data collection, and study documentation.
  • Help organize and prioritize study activities to meet project timelines and research objectives.
  • Support regulatory compliance by maintaining study records and adhering to protocol and institutional requirements.
  • Collaborate with research teams to ensure accurate, efficient, and compliant study operations.
  • Contribute to the successful conduct of clinical research in a fast paced, team oriented environment.

Job description

Description

The Assistant Clinical Research Coordinator supports the day to day operations of clinical research studies and works closely with Clinical Research Coordinators and Senior Clinical Research Coordinators to ensure the successful implementation of research activities. This role assists with study coordination, project management, and administrative tasks while helping to maintain compliance with study protocols and applicable regulatory requirements.

Key Responsibilities:
  • Support the implementation and coordination of one or more clinical research studies.
  • Assist with participant recruitment, study visits, data collection, and study documentation.
  • Help organize and prioritize study activities to meet project timelines and research objectives.
  • Support regulatory compliance by maintaining study records and adhering to protocol and institutional requirements.
  • Collaborate with research teams to ensure accurate, efficient, and compliant study operations.
  • Contribute to the successful conduct of clinical research in a fast paced, team oriented environment.

This position is an excellent opportunity for individuals interested in building a career in clinical research while gaining hands on experience supporting innovative studies and advancing patient focused research.

Note, this is a limited position, which may convert to career.

Salary: $27.08 - $43.55 hourly

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