Assistant Study Coordinator (LAUNCH Program)
Company: University of California - Los Angeles Health
Location: Santa Monica
Posted on: May 30, 2025
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Job Description:
DescriptionAs the Assistant Study Coordinator for the LAUNCH
program, you will assist the Clinical Research Coordinator and/or
Senior Clinical Research Coordinator in contributing to the overall
operational management of clinical research/trial/study activities.
In this role, you will recognize and perform necessary tasks to
assist the Clinical Research Coordinator and/or Senior Clinical
Research Coordinator in managing projects and prioritizing work to
meet necessary deadlines. You will support the Clinical Research
Coordinator and/or Senior Clinical Research Coordinator in planning
and organizing necessary tasks to ensure adherence to the study
protocol and applicable regulations. The full salary range for this
position is $27.08 - $43.55/Hourly. The budgeted salary that the
University reasonably expects to pay for this position is
$27.08/Hourly.
This is one of six open positions. By applying to this posting,
you'll be considered for all available opportunities.
Please note that this is a full-time 12-month limited position and
may convert to career.
Salary Range: $27.08 - $43.55/Hourly
QualificationsRequired:
Minimum of 1+
years of experience in a clinical research setting.
Interpersonal
skillstoeffectively communicate information in a timely,
professional manner andestablish 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 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.
Closeattentionto
detailto ensure accuracy in a fast-paced, fluctuating workload
environment.
Organization
skillsto create and maintain administrative and regulatory
files
effectively as well as independently balance the various tasks to
ensure
deadlines are met.
Demonstrated
proficiency withAdobe and Microsoft suite software, especially
Excel, to perform daily tasks efficiently and accurately.
Alearning
and professional growth mentalityso that new software tools,
systems, and processes can be adopted quickly and efficiently.
Workingknowledge
of clinical research concepts, policies and procedures, and human
safety
protection regulations and laws.
Knowledge of
and experienceworking 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 skillsto effectively establish
rapport,
building collaborative relationships, and communicate complex
concepts and
ideas in an easy-to-understand manner.
Ability
toadapt to changing job demands and priorities,
remainflexibleincluding working flexible hours to accommodate
research deadlines.
Ability to
handleconfidential informationwith judgement and
discretion.
High degree
ofconcentrationand focusin 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.
Keywords: University of California - Los Angeles Health, Compton , Assistant Study Coordinator (LAUNCH Program), Other , Santa Monica, California
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