Senior Clinical Documentation Specialist
hace 4 semanas
Job Title: Senior Clinical Documentation Specialist
About the Role:
As a Senior Clinical Documentation Specialist at ICON, you will be responsible for managing and maintaining Trial Master File (TMF) documentation. This will involve working closely with global study teams and other TMF Operations staff to ensure the accurate and timely processing of documents.
Key Responsibilities:
Review and process TMF documentation
Liaise with global study teams and other TMF Operations staff
Ensure accurate and timely processing of documents
Requirements:
Complete Bachelor's Degree in Health Sciences or related area
2+ years of experience in TMF management
Advanced English language skills
Competent computer skills
Benefits:
At ICON, we offer a competitive salary package and a range of health-related benefits to our employees and their families. We are an equal opportunity employer and are committed to providing a workplace free of discrimination and harassment.
Why ICON?
We are a world-leading healthcare intelligence and clinical research organization. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives.
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