
Lead Clinical Research Coordinator
20 hours ago
Job Summary:
We are seeking a Clinical Research Associate to support our clinical trial operations. The ideal candidate will have experience in authoring and analyzing clinical trial documents, working with key clinical documents, and collaborating with cross-functional teams.
Main Responsibilities:- Author and analyze clinical trial documents to ensure compliance with regulatory standards.
- Work with key clinical documents: Protocol, Informed Consent Form, Clinical Study Report, Summary of Clinical Safety/Efficacy, Access Evidence Dossier, Statistical Analysis Plan.
- Create, validate, and refine prompts for AI-assisted document generation to improve document accuracy and efficiency.
- Apply knowledge of clinical trial phases, study design, and drug development to ensure high-quality deliverables.
- Maintain quality control and ensure timely delivery of assigned tasks to meet project milestones.
- Collaborate with cross-functional teams to improve document accuracy and prompt effectiveness, and provide regular updates on project progress.
- Junior Role (6months - 4 years)
Location: Bengaluru, India
Country Code: IN
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