Medical Document Specialist
4 days ago
About us:
We are a global company that partners with major firms in various industries.
Job Title: Clinical Research Associate
Key Responsibilities:
- Author and analyze clinical trial documents.
- Work with key clinical documents: Protocol, Informed Consent Form, Clinical Study Report, Summary of Clinical Safety/Efficacy, Access Evidence Dossier, Statistical Analysis Plan 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.
Our ideal candidate will have 1-5 years of experience, any graduation qualification, and a strong understanding of clinical trials and regulations.
What We Offer:
• A dynamic work environment with opportunities for growth and professional development.
• Collaborative team atmosphere with experienced professionals.
• Flexible working arrangements to suit individual needs.
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