Clinical Research Coordinator - Flexible Hours & Travel

University of California - Los Angeles Health; Santa Monica (CA); On-site; USD 52,000 - 84,000; Full time

Job summary

University of California - Los Angeles Health is seeking a Clinical Research Coordinator to support the operational management of clinical studies from design through closeout. Responsibilities include prioritizing tasks, ensuring protocol compliance, and coordinating with investigators, departments, sponsors, and external sites to meet deadlines.

The role emphasizes collaboration, regulatory awareness (FDA CFR, ICH GCP), and strong communication with patients and team members.

Qualifications

• Bachelor's degree in related area or equivalent combination of education and experience.
• Minimum 2 years of clinical research/coordinator experience.
• Strong interpersonal skills to communicate professionally and collaborate with diverse teams.
• Ability to communicate with patients compassionately and clearly.
• Ability to manage priorities and meet deadlines under interruptions and regulatory requirements.
• Attention to detail in regulatory files and study documentation.
• Proficiency with Adobe and Microsoft Office tools to perform daily tasks.

Responsibilities

• Oversee operational management of clinical research activities across study lifecycle.
• Implement and manage research activities for one or more studies.
• Plan and organize study activities to meet deadlines and regulatory requirements.
• Ensure compliance with study protocols, FDA CFR, and ICH GCP.
• Collaborate with Principal Investigator, departments, sponsors, and external sites to support compliant study conduct and staffing.

Skills

Interpersonal skills

Prioritization

Communication with patients

Teamwork

Organization

Analytical skills

Attention to detail

Adaptability

Education

Bachelor's degree or equivalent

Tools

Adobe

Microsoft Excel

Job description

University of California - Los Angeles Health is seeking a Clinical Research Coordinator to support the operational management of clinical studies from design through closeout. Responsibilities include prioritizing tasks, ensuring protocol compliance, and coordinating with investigators, departments, sponsors, and external sites to meet deadlines.

The role emphasizes collaboration, regulatory awareness (FDA CFR, ICH GCP), and strong communication with patients and team members.