Study Coordinator

University of California - Los Angeles Health; Los Angeles (CA); On-site; USD 50,000 - 81,000; Full time

Job summary

The University of California - Los Angeles Health in Los Angeles is seeking a Clinical Research Coordinator to support cardiology studies. You will oversee day-to-day coordination from start-up through closeout, ensuring protocol compliance and adherence to FDA and ICH-GCP guidelines.

Collaborate with investigators, sponsors, and cross-functional teams on multiple priorities. Ideal candidates bring a Bachelor's degree or 1–3 years of coordination experience, plus strong communication and

Qualifications

• Bachelor's Degree or 1–3 years of study coordination experience.
• Strong verbal and written communication and interpersonal skills.
• Excellent organizational abilities to manage multiple projects and deadlines.
• Analytical skills to identify problems and propose solutions.
• Ability to adapt to changing demands and work flexible hours.
• Budgeting knowledge for clinical trial budgets.
• Working knowledge of FDA CFR and ICH GCP for clinical research.

Responsibilities

• Coordinate start-up through closeout of clinical studies in Cardiology.
• Ensure compliance with study protocols, FDA regulations and ICH-GCP guidelines.
• Collaborate with investigators, sponsors, and multidisciplinary teams while managing multiple priorities.

Skills

Communication

Organizational skills

Time management

Budgeting basics

FDA CFR knowledge

Education

Bachelor's degree

Job description

Description

The Department of Medicine is seeking a highly organized and detail-oriented Clinical Research Coordinator to support clinical research studies within the Division of Cardiology. In this role, you will oversee the day-to-day coordination of studies from start-up through closeout, ensuring compliance with study protocols, institutional policies, FDA regulations, and ICH Good Clinical Practice (GCP) guidelines. Working collaboratively with investigators, sponsors, and multidisciplinary research teams, you will play a key role in advancing innovative clinical research while managing multiple priorities in an academic medical center.

Hourly range: $36.37-$58.52

Qualifications

Required:

• Bachelors Degree or 1-3 years of previous study coordination or clinical research coordination experience.
• Strong verbal and written communication skills along with strong interpersonal skills to effectively establish rapport, and build collaborate relationships.
• Strong organizational capabilities to organize multiple projects and competing deadlines for efficiency and cost-effectiveness..
• Analytical skills sufficient to work and solve address problems and identify solutions with reasoned judgment.
• Ability to adapt to changing job demands and priorities; work flexible hours to accommodate research deadlines.
• Mathematical skills Sufficient to prepare clinical research budgets, knowledge of math ability and knowledge of clinical trials research budgeting process to assist with the preparation of clinical trial budgets.
• Working knowledge of FDA Code of Federal Regulations (CFR) and ICH Good Clinical Practice (GC) for clinical research.