Research Compliance Assistant In Illinois Job Details

Department: Regional Cancer Center
Category: Professional
Schedule: Part Time
Shift: Days
Hours: 8:00 a.m. - 4:30 p.m. (~ 24 hours a week)

Process receipt and maintain associated documentation for approved clinical trials being conducted at Memorial Health Systems.  Perform data entry of clinical trials in large Access database and maintain electronic clinical trial records. Assist with clinical trial billing functions including trial initiation and set up, process trial participant notifications, and maintain billing records.  Perform chart audits to assure compliance with documentation requirements.

Requirements for the position include:

1.     Minimum of an associate's degree or 4 years of equivalent experience in life science or related healthcare field required.  Previous clinical research experience preferred.

2.            Advanced computer skills including ability to work with computerized databases.

3.            Minimum of 2 years experience in clinical data management (preferred).

4.            Knowledge of federal and state regulatory requirements for human subjects protection and health information privacy.

5.            Skills to understand hospital billing processes, coding and financial regulations.

6.            Interpersonal and written communication skills.

7.            Able to make objective judgments.

8.            High degree of organizational skills including effective time management to set/reset priorities accordingly.

9.            Obtain and maintain human subjects protection education.

Date posted: 07/11/2010