Clinical Document Specialist Intern - job 1 of 2

Job Summary

A company is looking for a Student Worker - Clinical Document Specialist.

Key Responsibilities

• Assist with organizing, naming, and filing documents within the eTMF system
• Perform clinical trial document quality control (QC) checks to ensure accuracy and compliance
• Support TMF reconciliation and audit readiness efforts

Required Qualifications

• Currently enrolled in a graduate program in Life Sciences, Public Health, Regulatory Affairs, Clinical Research, or a related field
• Minimum GPA of 3.0 preferred
• Familiarity with document management systems or cloud-based platforms
• Ability to learn and follow structured processes and SOPs
• Interest in clinical trials, regulatory compliance, or pharmaceutical development