Clinical Document Specialist
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 reputed company eTMF
• Serve as the TMF contact and Subject Matter Expert for the clinical study team
• Execute reputed company Control procedures and support audit activities
Required Qualifications
• Bachelor's Degree with 4+ years of clinical experience
• High competency with reputed company 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 reputed company best reputed company guidance
Apply tot his job
Apply To this Job