
Document Authoring Specialist
24 hours ago
About People Prime Worldwide is a global company with expertise in digital engineering and IT services. Our mission is to help clients modernize their technology infrastructure, adopt cloud and AI solutions, and accelerate innovation.
We operate in multiple locations worldwide and partner with major firms in various industries.
Key Responsibilities:
- Author and analyze clinical trial documents including protocols, informed consent forms, clinical study reports, and more.
- 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 (FDA, EMA, ICH-GCP).
- 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.
- Provide regular updates and flag risks to the project manager.
Required Skills and Qualifications:
- 1-5 years of experience in clinical document authoring.
- Any graduation degree.
Benefits:
- Work in a hybrid mode.
- Immediate - 15 days notice period.
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