
Clinical Documentation Specialist
5 days ago
About People-Prime-Worldwide:
We are a global IT services company with 35,000+ associates worldwide, specializing in digital engineering and IT services. Our clients include major firms in banking, healthcare, telecom, and media.
Our team is known for combining deep industry expertise with agile development practices, enabling scalable and cost-effective digital transformation.
Clinical Document Authoring Job Description
- Job description: We are seeking a Clinical Research Associate to author and analyze clinical trial documents.
- Key responsibilities: You will work with key clinical documents, including protocols, informed consent forms, clinical study reports, and more.
- You will create, validate, and refine prompts for AI-assisted document generation.
- You will apply your knowledge of clinical trial phases, study design, and drug development to maintain compliance with global regulatory standards.
- You will utilize medical terminologies and ontologies for clarity and consistency.
- You will ensure quality control and timely delivery of assigned tasks.
- You will collaborate with cross-functional teams to improve document accuracy and prompt effectiveness.
- You will provide regular updates and flag risks to the project manager.
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