Clinical Document Agent

Role & responsibilities :

• Understanding of Clinical Trial documentation
• Phase 1 experience is must
• Knowledge of Investigator Site Files (ISF)
• Must have exp in Document QC
• Must have experience in Excel, creating forms and creating source documentation in Excel
• Knowledge adobe, computer skills
• Excellent Communication skills
• Ability to coordinate with cross-functional global teams

Ability to understand requirements and translate them into

documentation