
Clinical Content Specialist
3 days ago
About Our Project:
We collaborate with a global services company, specializing in digital engineering and IT solutions.
Our team operates in multiple locations across various countries, has delivery centers globally, and is backed by leading investors.
Job Title: Clinical Document Authoring Specialist
Key Responsibilities:
- Author and analyze clinical trial documents.
- Work with key clinical documents, including Protocol, Informed Consent Form, Clinical Study Report, and more.
- Create, validate, and refine prompts for AI-assisted document generation.
- Apply knowledge of clinical trial phases, study design, and drug development.
- Maintain compliance with global regulatory standards.
- Utilize medical terminologies and ontologies for clarity and consistency.
- Ensure quality control and timely delivery of assigned tasks.
- Collaborate with cross-functional teams to improve document accuracy and prompt effectiveness.
Benefits:
- A dynamic work environment
- Opportunities for career growth and professional development
- A competitive compensation package
Contact us today to learn more about this exciting opportunity
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