
Clinical Trials Expert
2 days ago
Clinical Research Associate Job Summary:
We are seeking an experienced Clinical Research Associate to join our organization. The successful candidate will have expertise in authoring and analyzing clinical trial documents.
Key Responsibilities:
- Author and analyze clinical trial documents.
- Work with key clinical documents, including protocols, informed consent forms, and clinical study reports.
- 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.
The ideal candidate will be able to work effectively in a hybrid environment and possess excellent communication and problem-solving skills.
Requirements:
- 1-5 years of experience in a related field.
- Any graduation qualification.
- Location: Meerut, India.
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