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Department: | Research Management Department |
Location: | San Antonio, TX |
Position Type: | FULL TIME |
SCOPE: Under minimal supervision, is responsible for the collection, coordination, processing and quality control of clinical trial data. May assist with screening patients for research protocols. Maintains research protocol information, regulatory documents and other research files as applicable. Works in compliance with Urology San Antonio Research Department (USARD) Standard Operating Procedure (SOP), principles of Good Clinical Practice and all applicable federal, state, and local regulations.
ESSENTIAL DUTIES AND RESPONSIBILITIES:
MINIMUM QUALIFICATIONS: High school diploma or equivalent required, some college coursework or other relevant background preferred. Three-five years of medical office experience (preferably in oncology or urology) and knowledge of medical terminology required. Minimum three years of experience as data coordinator required. SoCRA or ACRP certification preferred.
PHYSICAL DEMANDS: The physical demands described here are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. While performing the duties of this job, the employee is regularly required to experience prolonged sitting, some bending, stooping and stretching. Requires eye-hand coordination and manual dexterity sufficient to operate a keyboard, photocopier, telephone, calculator and other office equipment. Requires normal range of hearing and vision correctable to 20/20. Requires occasional lifting of up to 30 pounds.