Clinical Research Coordinator

• Coordinate and manage clinical trials from initiation to completion, ensuring compliance with regulatory requirements and company policies.
• Develop and maintain study protocols, case report forms, and other study-related documents.
• Collaborate with cross-functional teams, including investigators, data managers, and medical writers.
• Conduct site feasibility assessments and coordinate with investigators to ensure successful trial execution.
• Manage and track study progress, identifying and mitigating potential risks and issues.
• Ensure accurate and timely reporting of study data, including progress updates and final study reports.

Disclaimer: This job posting has been aggregated from external source. Role details, content, and availability are subject to change. Applicants are advised to confirm the latest information directly on the company website before applying.