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General Information

Work Location: Los Angeles, USA
Onsite or Remote
Flexible Hybrid
Work Schedule
TBD
Posted Date
11/20/2024
Salary Range: $30.56 - 60.82 Hourly
Employment Type
4 - Staff: Limited
Duration
1 year
Job #
20914

Primary Duties and Responsibilities

The Clinical Trials Analyst is responsible for regulatory coordination of clinical research studies within assigned units, departments or divisions. You will perform detailed review of clinical research protocols and utilize that information to prepare, manage and submit all required study/regulatory documents and all required applications and forms related to internal UCLA requirements, FDA requirements, sponsor requirements, etc. You will work with study monitors to process, review, and collect the appropriate regulatory documents in a timely manner and in compliance with federal, state, and university mandated regulations and policies. 


Salary Range: $30.56 - $60.82/Hourly


Please note, this is a part-time, one year limited position that may convert to career.

 

Job Qualifications

Required: 

  • Minimum of 1+ years of experience as a clinical researcher.
  • 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 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 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.


Preferred:

  • Bachelor’s degree.