UC San Diego Health · 12 hours ago
Assistant Clinical Research Coordinator - 136506
UC San Diego Health is a leading healthcare institution, and they are seeking an Assistant Clinical Research Coordinator. The role involves recruiting subjects and collecting clinical data for studies, managing clinical trials, and ensuring compliance with research protocols.
Health Care
Responsibilities
Responsible for coordinating and managing clinical trials including providing all aspects of protocol management, including screening for patient eligibility, data collection and analysis, ensuring protocol compliance, adverse drug reaction reports, laboratory and specimen submission, and maintenance of accurate and complete clinical research files
Assist the regulatory department with Human subjects submissions, renewals, and safety reports
Directly communicate with assigned physicians and disease groups
Provide direct assistance to the Project Manager in reviewing and verifying university research account statements, professional fee statements, and invoicing
Qualification
Required
Theoretical knowledge of biology, microbiology, social sciences, clinical sciences as typically attained by a Bachelor's degree, or an equivalent combination of education and experience
Experience performing clinical research duties in a clinical research environment
Experience using statistical software applications. Knowledge of database, word processing and spreadsheet applications such as Velos, Access, Excel and MS Word
Experience with clinical trials participant or study subject recruitment
Experience maintaining files and keeping records
Excellent planning and organizational skills and ability to work in a changing, multiple-demand setting in order to prioritize a large volume of work and meet deadlines efficiently and accurately
Excellent interpersonal, as well as written and verbal communication skills (using grammatically correct written English and accurate typing) to interact with a diverse population. Excellent phone etiquette skills
Ability to work independently. Ability to maintain confidentiality
Demonstrated ability to interact effectively with diverse groups, including professional and non-professional staff and clients
Preferred
Certification as a Clinical Research Associate or Coordinator
Experience working with research bulk accounts
Experience with investigational drug authorization criteria
Ability to speak, read, and write in Spanish
Experience interpreting medical charts, experience in abstracting data from medical records
Knowledge of National Institute of Health (NIH), Good Clinical Practice (GCP), Injury and Illness Prevention Program (IIPP), Human Resource Protection Program (HRPP), IATA Shipping of Blood Specimens, and Bloodborne Pathogens
Experience coordinating study startup activities
Experience providing in-service training to various research personnel on protocols, processes, and procedures
Experience completing clinical trials case report forms via hard copy and online
Company
UC San Diego Health
UC San Diego Health is the only academic health system in the San Diego region.
Funding
Current Stage
Late StageTotal Funding
$0.2MKey Investors
The Beryl InstituteThe Conrad Prebys Foundation
2025-10-31Grant
2023-06-26Grant· $0.2M
Recent News
2025-11-08
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