
Clinical Trial Specialist
1 day ago
About Us:
We are a global IT services company specializing in digital engineering and IT services. Our mission is to deliver innovative solutions to our clients.
Job Title: Clinical Research Associate
Key Responsibilities:
- Author and analyze clinical trial documents.
- Work with key clinical documents such as 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.
- 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.
Requirements:
- Bachelor's Degree or Higher
- 1 - 5 Years of Experience
Working at our company means working on exciting projects with talented colleagues from all over the world. We're always looking for skilled professionals who can contribute to our mission.
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