Clinical Research Coordinator — Regenerative Medicine

UC San Diego Health

San Diego (CA)

On-site

USD 85,000 - 137,000

Full time

7 days ago
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Job summary

UC San Diego Health is seeking professionals for its Sanford Stem Cell Institute at UC San Diego. The role involves coordinating clinical research activities, managing protocols, and supporting multi-disciplinary teams in regenerative medicine initiatives.

You will work with physicians and researchers to screen patients, collect samples, and ensure compliance with regulatory standards. The ideal candidate has a strong foundation in clinical trials, data management, and protocol design, with

Qualifications

  • Bachelor's Degree in biology or related field, or equivalent education and experience.
  • Experience in clinical research in CRO, academic or hospital settings.
  • Experience with screening patients, initiating treatment, collecting specimens, and orienting physicians.
  • Ability to work independently and escalate when needed.
  • Experience in clinical trials, protocols, data gathering and evaluation.
  • Experience with start-up procedures including feasibility, activation and IRB processes.
  • Knowledge of investigational protocols, data management and queries.
  • Ability to lead and support a research team with instruction and judgment.
  • Strong knowledge of medical terminology and documentation.

Skills

Clinical research
IRB processes
Data management
Protocol design
Communication skills
Time management
Team leadership
Problem solving
Medical terminology

Education

Bachelor's degree in Biology

Job description

UC San Diego Health is seeking professionals for its Sanford Stem Cell Institute at UC San Diego. The role involves coordinating clinical research activities, managing protocols, and supporting multi-disciplinary teams in regenerative medicine initiatives.

You will work with physicians and researchers to screen patients, collect samples, and ensure compliance with regulatory standards. The ideal candidate has a strong foundation in clinical trials, data management, and protocol design, with

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