Study Research Coordinator - Rheumatology

Responsibilities
As the Study Research Coordinator, you will assist with all active study activities for the division of Rheumatology. Primary duties include:

*Draw blood from clinical research patients
*Assist in the set-up, coordination, and management of the Industrial, Sponsor and Investigator-Initiated Studies, clinical trials and research activities
*Prepare and maintain required study & regulatory binders
*Process and maintain HSPC/IRB/FDA, sponsor and internal regulatory documentations
*Coordinate participant recruitment and enrollment and data collection; maintain study databases

Qualifications
*Must have current, California CPT certification
*Knowledge of subject recruitment, participant contact, consent, data collections
*Knowledge of normal and abnormal symptomatology and life threatening medical problems
*Ability to assist in medical emergencies and office procedures
*Knowledge of medical terminology, including safety requirements when handling Biohazardous specimens or contaminated instruments
*Strong interpersonal and communication skills to interact effectively, verbal and written
*Ability to collect pertinent information from study participants through interviews, surveys and questionnaires

A bonus if you have the following:
*A medical assistant diploma/certificate
*Knowledge in obtaining vital signs
*Skill in performing a 12-lead EKG
*Ability to push, pull or carry 30 lbs. or more
*Experience using CareConnect
UCLA is an Equal Opportunity/Affirmative Action employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected Veteran status.

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