Clinical Document Specialist

Job Summary

A company is looking for a Clinical Document Specialist to support the Clinical Operations department in trial document management.

Key Responsibilities

• Manage the lifecycle of clinical trial documentation in the Veeva eTMF
• Serve as the TMF contact and Subject Matter Expert for the clinical study team
• Execute Quality Control procedures and support audit activities

Required Qualifications

• Bachelor's Degree with 4+ years of clinical experience
• High competency with Veeva VAULT eTMF and knowledge of the TMF Reference Model
• Experience in organizing and coordinating electronic Trial Master Files
• Strong time management skills to handle competing priorities
• Ability to work independently and provide best practice guidance