Description
As 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
Qualifications
Required:
- 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.
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University of California - Los Angeles Health
May 29, 2025