
Clinical Trial Document Author
1 day ago
The role of a Document Authoring Specialist is crucial in clinical trial document management. In this position, you will be responsible for creating and analyzing documents that are critical to the success of clinical trials.
Key Responsibilities:
- Author and analyze clinical trial documents.
- Collaborate with cross-functional teams to improve document accuracy and prompt effectiveness.
- Apply knowledge of clinical trial phases, study design, and drug development.
- Maintain compliance with global regulatory standards (FDA, EMA, ICH-GCP).
- Utilize medical terminologies and ontologies for clarity and consistency.
- Ensure quality control and timely delivery of assigned tasks.
Requirements:
- Experience: 1-5 years
- Education Qualification: Any Graduation
Benefits include collaboration with cross-functional teams and opportunities for professional growth.
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