Clinical Research Assistant - Los Angeles, United States - Global Healthcare IT

Global Healthcare IT
Global Healthcare IT
Verified Company
Los Angeles, United States

3 weeks ago

Mark Lane

Posted by:

Mark Lane

beBee recruiter
Description

Previous experience with quality control required

Previous experience with Clinical Research/Trials required
BIMO/FDA Audit Work/Collaboration
Process Improvement
Study Start Up/Close Out

Work Experience:

  • 1+ yrs experience in outpatient clinical setting required
  • 1+ yrs. in a managed care environment; clinical experience as an MA or Nurse preferred
  • 2+ yrs of research experience with Quality emphasis required

Job Summary:


The role of the Program Assistant is to support various programs and day-to-day administrative functions that support the department and the Executive Director to ensure the success of all initiatives.


Duties include:


  • Monitor and manage all referral requests/ques to ensure clinical information is provided and/or authorized, and provide feedback to ordering providers or when submitting to the Health plan (whichever is applicable).
  • Develop strong partnership with liaisons, providers, and all others one has direct contact with on a daily basis.
  • Serve as a liaison between the department, CSMCF Providers, and/or staff and the Management team.
  • Develop system to track project outcomes and consistently provide feedback/updates to Management team.
  • Implement LEAN methodology into daily workflow.


These statements describe the primary duties and responsibilities of the job and are not intended to be an exhaustive list of all tasks.

Other work duties may be assigned at any time with or without notice.


Education:


  • HS Diploma/GED minimum
  • AA Degree, Trade Tech, or BA Degree preferred

Pay:
$ $28.00 per hour


Benefits:


  • 401(k)
  • 401(k)
matching

  • Dental insurance
  • Health insurance
  • Paid time off
  • Vision insurance

Schedule:

  • 8 hour shift
  • Day shift
  • Monday to Friday

Education:


  • Bachelor's (preferred)

Experience:


  • Clinical research/trials: 1 year (required)
  • Outpatient clinical settings: 1 year (required)
  • Managed care environment: 1 year (preferred)
  • Research experience with quality emphasis: 2 years (required)
  • BIMO/FDA Audit Work/Collaboration: 1 year (preferred)
Process Improvement: 1 year (preferred)

  • Study Start Up/
Close Out: 1 year (preferred)


Ability to Relocate:

  • Los Angeles, CA 90025: Relocate before starting work (required)

Work Location:
In person
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