
Clinical Research Expert
2 days ago
About our client:
We are a global company headquartered in the US, founded in 1996. We specialize in digital engineering and IT services, helping clients modernize their technology infrastructure and adopt cloud and AI solutions.
Our team is known for combining deep industry expertise with agile development practices, enabling scalable and cost-effective digital transformation. We operate in over 50 locations across more than 25 countries.
Key Responsibilities:
- Author and analyze clinical trial documents.
- Work with key clinical documents such as Protocol, Informed Consent Form, Clinical Study Report, Summary of Clinical Safety/Efficacy, Access Evidence Dossier, Statistical Analysis Plan.
- 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.
Requirements:
- 1-5 years of experience
- Any Graduation
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