
Clinical Document Specialist
6 days ago
We are seeking a skilled Clinical Research Associate to join our team. As a Clinical Research Associate, you will be responsible for authoring and analyzing clinical trial documents.
The ideal candidate will have knowledge of clinical trial phases, study design, and drug development. They will also possess strong analytical skills and the ability to create, validate, and refine prompts for AI-assisted document generation.
The successful candidate will be able to maintain compliance with global regulatory standards (FDA, EMA, ICH-GCP) and utilize medical terminologies and ontologies for clarity and consistency.
In addition to these responsibilities, the Clinical Research Associate will ensure quality control and timely delivery of assigned tasks. They will also collaborate with cross-functional teams to improve document accuracy and prompt effectiveness.
Key Responsibilities:
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