
Clinical Research Document Expert
4 days ago
Clinical Research Document Expert
">We are seeking a skilled Clinical Research Document Expert to join our team. This individual will be responsible for creating and analyzing clinical trial documents, working with key clinical documents such as protocols, informed consent forms, and clinical study reports.
">Key Responsibilities:
- Author and analyze clinical trial documents to ensure compliance with regulatory standards.
- Collaborate with cross-functional teams to improve document accuracy and prompt effectiveness.
- Utilize medical terminologies and ontologies for clarity and consistency.
- Maintain quality control and timely delivery of assigned tasks.
- Work with hybrid teams to create, validate, and refine prompts for AI-assisted document generation.
Requirements:
- 1-5 years of experience in a related field.
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