New

Study Coordinator

University of California - Los Angeles Health

United States, California, Los Angeles

Jan 14, 2026

Description

The Department of Medicine is hiring a Clinical Research Coordinator within the Division of Pulmonary Medicine to support the full lifecycle of clinical research studies, from design and setup to conduct and closeout. This role is responsible for implementing research activities, managing multiple projects, and prioritizing tasks to meet deadlines while ensuring strict adherence to study protocols and regulatory requirements, including institutional policies, FDA regulations, and ICH Good Clinical Practice (GCP).

The Clinical Research Coordinator works closely with research teams, ancillary departments, sponsors, and other stakeholders to ensure smooth study operations. Responsibilities include coordinating study activities, maintaining compliance, supporting financial management, and providing adequate personnel support to ensure the successful execution of clinical trials.

Hourly Range: $35.31-$56.82

Qualifications

Required:

Bachelors Degree or 1-3 years of previous study
coordination or clinical research coordination experience
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.
Ability to respond to situations in an
appropriate and professional manner.
Ability to concentrate and focus in a work
environment that contains distracting stimuli and competing deadlines.
Ability to be flexible in handling work
delegated by more than one individual.
Typing and computer skill/ability including
word-processing, use of spreadsheets, email, data entry. Ability to navigate
numerous software programs and applications.
Ability to handle confidential material
information with judgement and discretion.
Working knowledge of FDA Code of Federal
Regulations (CFR) and ICH Good Clinical Practice (GC) for clinical research.
Be available to work in more than one
environment, travel to meetings, off-site visits, conferences, etc.
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.
Working knowledge of the clinical research
regulatory framework and institutional requirements.