Document Authoring Specialist
21 hours ago
Unlock Your Potential in Clinical Research and Document Authoring
About People Prime Worldwide:
We are a global IT services company that helps clients modernize their technology infrastructure and accelerate innovation.
Our expertise lies in combining deep industry knowledge with agile development practices, enabling scalable and cost-effective digital transformation.
Job Title: Clinical Document Authoring
About the Role:
The ideal candidate will be responsible for authoring and analyzing clinical trial documents to ensure accuracy and compliance with regulatory standards.
Key Responsibilities include working with key clinical documents such as protocols, informed consent forms, and clinical study reports.
Responsibilities also include creating, validating, and refining prompts for AI-assisted document generation using medical terminologies and ontologies.
The successful candidate will apply knowledge of clinical trial phases, study design, and drug development to maintain high-quality documents.
Additionally, they will collaborate with cross-functional teams to improve document accuracy and prompt effectiveness.
Requirements:
- 1-5 years of experience in clinical research or document authoring
- Any graduation degree is required
Join Our Team
As a leading global IT services company, we operate in over 50 locations across more than 25 countries. We offer a hybrid work mode for our employees. Interested candidates can share their CVs for consideration.
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