
Research Operations Specialist
2 days ago
About People Prime Worldwide is no longer relevant to this job description.
We specialize in digital engineering and IT services. Our expertise helps clients modernize technology infrastructure, adopt cloud and AI solutions, and accelerate innovation.
Job Title: Clinical Research Associate
Key Responsibilities:
- Create clinical trial documents and analyze them for quality control.
- 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 and more.
- Develop, 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.
Beyond technical requirements, the successful candidate will ensure quality control and timely delivery of assigned tasks. This involves collaborating with cross-functional teams to improve document accuracy and prompt effectiveness.
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