
Clinical Documentation Specialist
14 hours ago
About Us:
Our firm is a global IT services company with expertise in digital engineering and IT solutions. We partner with leading firms across various industries.
Our mission is to help clients modernize their technology infrastructure, adopt cloud and AI technologies, and accelerate innovation through agile development practices.
We operate globally, with delivery centers in Asia, Europe, and North America.
Job Title: Clinical Document Authoring
Key Responsibilities:
- Author and analyze clinical trial documents.
- Work with key clinical documents such as protocol, informed consent form, clinical study report, 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.
Required Skills and Qualifications:
Candidates must have 1-5 years of experience, any graduation, and strong skills in protocol, informed consent form, FDA, EMA, ICH-GCP, and medical terminologies.
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