Study Coordinator

Job Description :

• Coordinate all aspects of clinical trials, from study initiation to study completion
• Manage and maintain study documentation, including case report forms, source documents, and ethics committee/regulatory submissions
• Ensure compliance with GCP guidelines and ethics committee (EC) requirements
• Recruit and screen potential study participants
• Obtain informed consent from study participants
• Collect and manage study data
• Monitor participant safety and report adverse events
• Maintain accurate and complete study records
• Prepare study reports and presentations
• Liaise with investigators, sponsors, EC and regulatory agencies

Job Specification :

• Medical Doctor
• Minimum of 2 years of experience working as a Clinical Research Coordinator or in a related clinical research role
• Strong understanding of Good Clinical Practice (GCP) guidelines and regulations
• Excellent organizational and time management skills
• Proficient in Microsoft Office Suite, electronic medical record (EMR) system, and electronic clinical trial software
• Ability to work independently and as part of a team
• Excellent communication and interpersonal skills