Job Details

Description

We are seeking anexperienced Budget Amendment Negotiator who will be responsible for regulatorycoordination of clinical research studies within assigned units, departments,or divisions. Perform detailed review of clinical research protocols andutilizes that information to prepare, manage all required Budget Amendment relatedsubmissions and all required applications and forms related to internal UCLArequirements, FDA requirements, sponsor requirements, etc. Work with industrypartners and ancillary teams to process, review and collect the appropriateregulatory documents in a timely manner and in compliance with federal, state,and university mandated laws, regulations and policies.

Hourly SalaryRange: $31.51 - $62.64

Required:

• Minimumof 1+ years of experience as a clinical researcher
• Interpersonalskills to effectively communicate information in a timely, professional mannerand establish and maintain cooperative and effective working relationships withstudents, staff, faculty, external collaborators and administration and to workas a member of a team.
• Abilityto set priorities and complete ongoing tasks with competing deadlines, withfrequent interruptions, to meet the programmatic and department needs, whilecomplying with applicable University policies and federal and stateregulations.
• Analyticalskills to assess clinical research protocols and regulatory requirements,define problems, formulate logical solutions, develop alternative solutions,make recommendations, and initiate corrective actions.
• Closeattention to detail to ensure accuracy in a fast-paced, fluctuating workloadenvironment.
• Organizationskills to create and maintain administrative and regulatory files effectivelyas well as independently balance the various tasks to ensure deadlines are met.
• Demonstratedproficiency with Adobe and Microsoft suite software, especially Excel, toperform daily tasks efficiently and accurately.
• Alearning and professional growth mentality so that new software tools, systems,and processes can be adopted quickly and efficiently.
• Workingknowledge of clinical research concepts, policies and procedures, and humansafety protection regulations and laws.
• Knowledgeof and experience working with a variety of local and external IRBs, scientificreview and other research committees, national cooperative group sponsors,industry sponsors, federal and foundation funding organizations, etc.

Preferred:

• Bachelor'sdegree