Interventional Clinical Trials Coordinator

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

Job summary

University of California - Los Angeles Health is seeking an experienced Clinical Research Coordinator to support interventional trials across multiple divisions. You will coordinate and manage study activities for drug and device trials, including participant recruitment, study implementation, data collection, and regulatory compliance.

Responsibilities include coordinating budgets, ensuring adherence to FDA CFR and ICH GCP guidelines, and collaborating with teams to meet deadlines while

Qualifications

• Bachelor's Degree or 1-3 years of prior study coordination or clinical research coordination experience.
• Strong verbal and written communication and interpersonal skills.
• Solid organizational skills to manage multiple projects and deadlines.
• Analytical abilities to identify problems and determine solutions.
• Ability to adapt to changing demands and work flexible hours for deadlines.
• Professional response to situations and discretion with confidential information.
• Working knowledge of clinical research regulatory framework and institutional requirements.
• Familiarity with FDA CFR and ICH GCP guidelines.

Responsibilities

• Coordinate and manage interventional clinical trials across divisions.
• Recruit participants and oversee study implementation and data collection.
• Ensure compliance with regulatory requirements and study protocols.
• Prepare budgets and support budgeting processes for trials.

Skills

Verbal communication

Written communication

Interpersonal skills

Organizational skills

Analytical skills

Adaptability

Time management

Data entry

Confidentiality

Education

Bachelor's degree

Job description

University of California - Los Angeles Health is seeking an experienced Clinical Research Coordinator to support interventional trials across multiple divisions. You will coordinate and manage study activities for drug and device trials, including participant recruitment, study implementation, data collection, and regulatory compliance.

Responsibilities include coordinating budgets, ensuring adherence to FDA CFR and ICH GCP guidelines, and collaborating with teams to meet deadlines while