Description
The
Assistant Clinical Research Coordinator assists the Clinical Research Coordinator
and/orSenior Clinical Research Coordinator in contributing to the
overall operational management of clinical research/trial/study activities. In this role, you will
perform necessary tasks to assist in managing projects and prioritizing work to meet necessary
deadlines. You will provide support in planning and organizing necessary tasks to ensure adherence to the
study protocol and applicable regulations. Hourly range: $29.28
- $47.10
Qualifications
Required:
- Minimum of 1+ years of experience in a
clinical research setting - Interpersonal skills to effectively
communicate information in a timely, professional manner and establish and
maintain cooperative and effective working relationships with students, staff,
faculty, external collaborators and administration and to work as a member of a
team. - Ability to effectively communicate to and
interact with patients in a compassionate and kind manner. - Ability to set priorities and complete ongoing
tasks with competing deadlines, with frequent interruptions, to meet the
programmatic and department needs, while complying with applicable University
policies and federal and state regulations. - Analytical skills to assess clinical research
protocols and regulatory requirements, define problems, formulate logical
solutions, develop alternative solutions, make recommendations, and initiate
corrective actions. - Close attention to detail to ensure accuracy
in a fast-paced, fluctuating workload environment. - Organization skills to create and maintain
administrative and regulatory files effectively as well as independently
balance the various tasks to ensure deadlines are met. - Demonstrated proficiency with Adobe and
Microsoft suite software, especially Excel, to perform daily tasks efficiently
and accurately. - A learning and professional growth mentality
so that new software tools, systems, and processes can be adopted quickly and
efficiently. - Working knowledge of clinical research
concepts, policies and procedures, and human safety protection regulations and
laws. - Knowledge of and experience working with a
variety of local and external IRBs, scientific review and other research
committees, national cooperative group sponsors, industry sponsors, federal and
foundation funding organizations, etc. - Strong verbal and written communication skills
to effectively establish rapport, building collaborative relationships, and
communicate complex concepts and ideas in an easy-to-understand manner. - Ability to adapt to changing job demands and
priorities, remain flexible including working flexible hours to accommodate
research deadlines. - Ability to handle confidential information
with judgement and discretion. - High degree of concentration and focus in a
work environment that contains distracting stimuli, competing deadlines, and
work delegated by more than one individual. - Availability to work in more than one
environment, travelling to various clinic sites, meetings, conferences, etc.
Preferred:
- Bachelor's Degree in related area and/or
equivalent combination of education and experience
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University of California - Los Angeles Health
Apr 10, 2026