• Provides general administrative assistance, including but not limited to organizational processes, materials management and data entry support.

• Maintains files, logs and other materials in an organized, efficient manner.

• Assists clinical research staff to assure all study requirements are documented and meet both internal and external regulations in accordance with protocol guidelines.

• Updates the Clinical Trials Management System (CTMS).

• Responsible for obtaining required signatures on clinical trial documents and returning within specified time frames.

• Candidate will receive additional supportive mentoring for skills development after initial orientation.

• Assignments will be determined by supervisor based on skills, training and competence levels.

• Assignments may broaden in complexity with experience requiring increasing self-directed activity.

• Responds to internal and external customer requests in a timely fashion.

• Assists with the coordination of sponsor visits.

• Performs data quality checks as needed.

• Performs other related duties as required and directed.

• High school diploma

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

Additional Information

• Schedule: Part-time
• Requisition ID: 24000451
• Daily Work Times: Standard Business Hours
• Hours Per Pay Period: 40
• On Call: No
• Weekends: No