Clinical Research Study Coordinator

University of California - Los Angeles Health; Los Angeles (CA); On-site; USD 43,000 - 69,000; Full time

Job summary

University of California - Los Angeles Health is seeking an Assistant Clinical Research Coordinator to support the Principal Investigator in daily operations of Neurology clinical studies. You will recruit participants, assist with informed consent, review medical charts, administer batteries, interview participants, and ensure regulatory documentation is up to date.

The role requires strong organization, discretion with confidential information, and the ability to manage multiple protocols and

Qualifications

• Ability to work efficiently and complete tasks with thoroughness and accuracy.
• Strong verbal and written communication skills and interpersonal abilities.
• Strong organizational capabilities and ability to manage deadlines across multiple protocols.

Responsibilities

• Assist with participant identification and recruitment under IRB-approved plans.
• Assist with informed consent process.
• Conduct medical chart reviews.
• Administer research batteries and interview study participants.
• Schedule participant visits and coordinate calendars.
• Maintain regulatory and study documentation per ethics guidelines.
• Procure study supplies and manage inventory.
• Support data entry and resolve queries across databases.

Skills

Time management

Communication

Organizational skills

Problem solving

Adaptability

Discretion

Data entry

Multitasking

Confidentiality

Information coordination

Tools

Word processing

Spreadsheets

Email

Job description

University of California - Los Angeles Health is seeking an Assistant Clinical Research Coordinator to support the Principal Investigator in daily operations of Neurology clinical studies. You will recruit participants, assist with informed consent, review medical charts, administer batteries, interview participants, and ensure regulatory documentation is up to date.

The role requires strong organization, discretion with confidential information, and the ability to manage multiple protocols and