
Study Documents Coordinator
4 days ago
A Study Documents Coordinator Role
">Job Description:- Responsibilities Include Document Processing, Collaboration with Study Teams, Project Execution and File Maintenance to Ensure Consistency and Accuracy in Study Files.
- Strong Understanding of Clinical Study Documentation and GCP Compliance.
- Excellent Oral and Written Communication Skills, Detail-Oriented with a Focus on Accuracy and Regulatory Compliance.
- Collaborative Ability to Work Effectively with Cross-Functional Teams, Clients, and Leadership.
- Document Receipt and Processing, Scanning, Indexing, Quality Control, Copying, Filing, Archiving, and Reporting.
- Provide Status Updates and Necessary Information for Client and Departmental Reports upon Request.
- Notify the Manager Regarding Training Needs, Project Activities, Quality Concerns, Timeline Risks, and Document Requests.
- Excellent Communication Skills.
- Proven Ability to Collaborate with Teams and Clients.
- Detail-Oriented with a Focus on Accuracy and Regulatory Compliance.
- Bachelor's Degree in Life Sciences (Preferred).
- Equivalent Experience in Clinical Documentation May Be Considered.
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Study Document Coordinator
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