I'm looking for a Clinical Research Associate (CRA) to ensure compliance and manage regulatory documentation for a clinical trial. Key Responsibilities: - Handle compliance and regulatory documentation - Manage patient information and clinical trial results Required Expertise: - In-depth knowledge of Good Clinical Practice (GCP), FDA Regulations, and ICH Guidelines - Experience in clinical trial compliance and regulatory documentation Ideal Skills: - Strong attention to detail - Excellent organizational skills - Prior experience as a CRA is a plus If you have the right qualifications and experience, please submit your proposal.
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