Impactful Neuroscience Clinical Research Coordinator

UC San Diego Health

San Diego (CA)

On-site

USD 85,000 - 137,000

Full time

14 days+

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Job summary

UC San Diego Health is seeking a motivated Clinical Research Coordinator to support investigations in epilepsy, neuroimmunology, and related CNS disorders across UCSD and Rady Children's Hospital. You will coordinate start-up, recruitment, data entry, and regulatory oversight while ensuring compliance with FDA/IRB requirements.

The role involves interaction with investigators, sponsors, and trial staff, development of regulatory documents, and use of Velos and Clinical Conductor for trial

Qualifications

  • Bachelor's degree in biology or related field or equivalent experience.
  • 3 years in clinical trials research; GCP and FDA regulations knowledge.
  • Experience with IRB, regulatory documents, and data entry.
  • Ability to manage multiple studies and vendors; strong communication.
  • Experience with start-up procedures, site activation, and regulatory processes.

Responsibilities

  • Coordinate start-up, implementation, recruitment, and enrollment.
  • Oversee regulatory compliance, IRB interactions, and consent forms.
  • Manage study documents, CRFs, and data entry across trials.
  • Liaise with UCSD/RCHSD departments, sponsors, and CROs.
  • Oversee scheduling, budgeting, and participation in trial operations.

Skills

GCP knowledge
FDA regulations
IRB processes
Data management
Regulatory documents
Communication

Education

Bachelor's Degree in Biology/related field
Equivalent experience considered

Tools

Velos
Clinical Conductor

Job description

UC San Diego Health is seeking a motivated Clinical Research Coordinator to support investigations in epilepsy, neuroimmunology, and related CNS disorders across UCSD and Rady Children's Hospital. You will coordinate start-up, recruitment, data entry, and regulatory oversight while ensuring compliance with FDA/IRB requirements.

The role involves interaction with investigators, sponsors, and trial staff, development of regulatory documents, and use of Velos and Clinical Conductor for trial

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