
Senior Clinical Document Analyst
1 week ago
About Clinical Research Associates:
We are a global firm with operations across 50+ locations worldwide, specializing in digital engineering and IT services.
We operate globally with delivery centers around the world. Our expertise combines deep industry knowledge with agile development practices.
Key Responsibilities:
- Analyze clinical trial documents and create AI-assisted document generation prompts.
- Work with key clinical documents: Protocol, Informed Consent Form, Clinical Study Report, Summary of Clinical Safety/Efficacy, and more.
- 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.
Requirements:
- 1-5 years of experience.
- Bachelor's degree or higher.
Job Benefits:
We offer opportunities for professional growth and collaboration with cross-functional teams.
Why Choose Us:
We provide regular updates and flag risks to project managers.
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