
Clinical Research Documentation Specialist
1 week ago
Document Authoring Professional
We are seeking a skilled and detail-oriented Document Authoring Professional to join our team.
About the Role:
- Author and analyze clinical trial documents with accuracy and efficiency.
- Collaborate with cross-functional teams to improve document quality and compliance.
- Develop and refine prompts for AI-assisted document generation.
- Apply knowledge of clinical trial phases, study design, and drug development to ensure high-quality documents.
- Maintain strict adherence to global regulatory standards (FDA, EMA, ICH-GCP).
- Utilize medical terminologies and ontologies to enhance document clarity and consistency.
- Provide regular updates and flag potential risks to project managers.
Requirements:
- 1-5 years of experience in clinical research or a related field.
- Any graduation degree.
Why This Role Matters:
This role plays a critical part in ensuring the accuracy and quality of clinical trial documents. As a Document Authoring Professional, you will be instrumental in driving the success of our projects by providing high-quality documents that meet regulatory requirements.
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