Clinical Research Assistant

Provides support to the clinical research coordinator or clinical research nurse. 

1. →Provides general administrative assistance, including but not limited to organizational processes, materials management and data entry support.
2. →Maintains files, logs and other materials in an organized, efficient manner.
3. →Assists clinical research staff to assure all study requirements are documented and meet both internal and external regulations in accordance with protocol guidelines.
4. →Updates the Clinical Trials Management System (CTMS).
5. →Responsible for obtaining required signatures on clinical trial documents and returning within specified time frames.
6. →Candidate will receive additional supportive mentoring for skills development after initial orientation.
7. →Assignments will be determined by supervisor based on skills, training and competence levels.     
8. →Assignments may broaden in complexity with experience requiring increasing self-directed activity.
9. →Responds to internal and external customer requests in a timely fashion.
10. →Assists with the coordination of sponsor visits.
11. →Performs data quality checks as needed.
12. →Performs other related duties as required and directed.

Required:

• High school diploma

Preferred: 

• Six months experience with data entry.
• Office experience in a medical setting.