Clinical Research Coordinator: Start-Up & Data Expert

San Diego Supercomputer Center; San Diego (CA); On-site; USD 50,000 - 80,000; Full time

Job summary

UC San Diego Health in La Jolla seeks an Assistant Clinical Research Coordinator to coordinate start-up, recruitment, enrollment, and maintenance of study subjects. You will support regulatory compliance, data handling, and communications with physicians.

Responsibilities include assisting investigators with proposals and reports, developing documents for disease teams, and ensuring adherence to HRPP/IRB and FDA requirements. Strong English communication is essential.

Qualifications

• Theoretical knowledge of biology, microbiology, clinical sciences or related field, or equivalent experience.
• Experience performing clinical research duties in a regulated environment.
• Familiarity with FDA regulations, NCI policies and Good Clinical Practice guidelines.
• Experience interpreting medical charts and abstracting data from medical records.
• Strong interpersonal and written/oral communication skills in English.
• Experience creating informed consent documents complying with HRPP/IRB, FDA, sponsor requirements.
• Proficiency with Microsoft Word and Excel for reporting and data management.

Responsibilities

• Coordinate start-up procedures, recruitment, screening, enrollment, and maintenance of subjects.
• Assist with regulatory compliance and data management for clinical trials.
• Communicate with investigators and coordinate with PIs on proposals, reports and manuscripts.
• Prepare documents, templates, and policies for disease teams.
• Work with regulatory officials as needed and maintain complete study files.

Skills

Biology knowledge

Clinical research

FDA regulations

HRPP/IRB policies

Data management

Communication skills

Informed Consent

Word processing

Education

Bachelor's degree or equivalent

Tools

Word

Excel

Job description

UC San Diego Health in La Jolla seeks an Assistant Clinical Research Coordinator to coordinate start-up, recruitment, enrollment, and maintenance of study subjects. You will support regulatory compliance, data handling, and communications with physicians.

Responsibilities include assisting investigators with proposals and reports, developing documents for disease teams, and ensuring adherence to HRPP/IRB and FDA requirements. Strong English communication is essential.