Clinical Research Coordinator

Job responsibilities

• Coordinate and support clinical research studies as per protocol, SOPs, and regulatory requirements.
• Maintain study-related documents, records, and essential documentation.
• Coordinate with investigators, study teams, sites, and other stakeholders.
• Support patient/subject recruitment, screening, scheduling, and follow-up activities.
• Ensure timely and accurate data collection and documentation.
• Assist with study visits, monitoring activities, and resolution of queries.
• Ensure compliance with GCP, protocol, and applicable regulatory requirements.