Hybrid 2 3 days remote, onsite location is 1000 Veteran Ave 32 59,Los Angeles, CA 90095. Possible ext past 26 weeks. REQUIRED Research Regulatory experience (amendment/continuing review submissions) Familiar with the IRB systems (Central exp. Advarra/WCG), Experience with the budget/contract side of research. PREFERRED Clinical research experience, Epic system, Microsoft S

Under the direction of principal investigator(s), this individual will serve as the programs manager for all projects under the Maternal and Child Health Center of Excellence (MCH CoE) within the UCLA Medicine Pediatrics and Preventive Medicine Division. The incumbent will provide programmatic support to the project directors in order to accomplish the goals of the projec

Local Rate Only. Onsite at 10920 Wilshire Blvd., Ste. 1700 Los Angeles, CA 90024. Required Exp Excel, Financial Planning and Analysis, Expense management. Preferred Exp Labor management (position control, FTE), healthcare experience

REQUIRED communicate professionally and effectively with physicians,staff, and patients in a high volume setting. Knowledge of major medical insurance plans, obtaining benefits and procedure authorizations. Knowledge of Microsoft Outlook, works and basic computer programs.

Under the general direction of the Department Research Associate (DRA), the Pre Award Fund Manager will provide support to Department of Medicine with preparing proposals for new funding opportunities, reviewing proposals to ensure compliance with University and funding agency guidelines, and be responsible for all financial and research administration for Principal Inves

The Clinical Trial Research Program is seeking a Fund Manager for the Department of Medicine Clinical Trials. In this role, you will oversee an assigned portfolio of accounts, prepare monthly financial statements, monthly ledger reconciliation for correctness and resolve to reverse and incorrect charges and follow up with clinical team and other servicing departments. You

STATEMENT Under the direction and supervision of the UM Assistant Manager, the Case Management Coordinator receives urgent, rountine, pre service and retro authorization requests and processes them through the referral and authorization procedures as established by the medical group utilization department. Responsible for prepping and processing referrals according to DOFR

REQUIRED Medical Front/Back Desk experience. Must have experience working with insurances & stated on the resume.

Medical Front/Back Desk experience, experience working with insurances. Parking is at the expense of the candidate. Candidate will be required to buy & wear a blue button down shirt.

Working knowledge of medical terminology, ICD 9, CM & CPT coding rules. Experience Charge Review, Clerical/Administration. Skills Attention to detail, analytical, organized, interpersonal communication, multitasking. Location currently hybrid on campus and at home. Schedule Monday Friday. 8 am 5 pm. Job Duties The Department of Medicine Clinical Trial Program is seeking a

The Clinical Trial Research Program is seeking an experienced Regulatory Project Manager to oversee, manage, and participate in startup research activities and be responsible for the oversight of regulatory coordination for clinical research studies. This includes being responsible for regulatory coordination of clinical research studies, preparation, submission and maint

Under the general supervision of the MSO and Division Chief, provide administrative support to the Division Co Chief. Maintain calendar and schedule meetings for division chief. Responsible for clerical and administrative duties as assigned by Division chief. Answer phones. Check mail. Other miscellaneous duties as assigned or required by the MSO and Division Co Chief. Qu

Check voicemail and respond to messages as needed. Perform daily HBS Time and Attendance review of Leaves of Absence, New Hires/Separations (Active Review), Retro Review which requires review of timesheets. Review report for separations, transfers, leaves of absence. Contact departments for approval of separation timesheets. Obtain documentation from Job Data to include i

Hybrid, but mostly remote. 700 Tiverton 8 684 Factor, Los Angeles, CA 90095 Must ask each candidate the following and include their answers on the BOTTOM of the cover sheet prior to submittal Do you have experience creating and updating study protocol calendars and budgets in a CRMS or CTMS? If yes, which application? Job Description Under the direction of the Clinical St

Essential to Research Position must be tied to essential research that is currently active and requires a unique qualification or specific skill set that is not easily transferable. This position is necessary to ensure the proper and timely reporting of research data collected on various research studies. This includes reporting of research data to sponsor and to the UCLA