
Medical Document Author
1 day ago
We are seeking a skilled Clinical Research Associate to join our team.
Job Description:
The successful candidate will be responsible for authoring and analyzing clinical trial documents, working with key clinical documents such as protocols, informed consent forms, and clinical study reports. They will also create, validate, and refine prompts for AI-assisted document generation.
- Author clinical trial documents and analyze them to ensure accuracy and compliance.
- Work with cross-functional teams to improve document accuracy and prompt effectiveness.
- Collaborate with project managers to provide regular updates and flag risks.
Required Skills and Qualifications:
To be considered for this role, applicants should have 1-5 years of experience in clinical research or a related field and any graduation qualification is required.
Benefits:
- Opportunities for professional growth and development.
- A chance to work on cutting-edge projects with our experienced team.
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