Jobs are sourced directly from employers. No recruiter involved. Apply through the employer’s link to make sure your application reaches the right people. → Clinical Research Coordinator
Main Responsibilities
1. Study Coordination and Support
• Prepare documents and reports for Institutional Review Board (IRB) review and approval.
• Develop case report forms (CRF) and other study data collection tools.
•Organize and deliver training for study staff on protocols, procedures, and regulatory requirements.
• Coordinate study activities at the clinical research site, including:
o Participant scheduling
o Informed consent processes
o Eligibility verification
o Treatment adherence monitoring
o Safety monitoring
• Coordinate participant recruitment, retention, and engagement efforts.
•Collaborate with healthcare facilities, research networks, and community partners to support study implementation.
• Maintain meticulous records and documentation of all study activities, participant data, and regulatory compliance.
•Prepare progress reports, technical reports, and other study documentation.
2. Quality Assurance and Compliance
•Develop Standard Operating Procedures (SOPs), quality control and quality assurance tools.
• Monitor daily study operations to ensure compliance with SOPs, Good Clinical Practice (GCP), and all applicable regulations.
•Review consent forms, participant records, adverse event reports, and other study documents to verify data quality and integrity.
3. Study Operations
•Develop plans for preparing research facilities, equipment, and staffing.
•Participate in the development of study budgets.
•Oversee administrative and logistical tasks at the clinical research site.
• Manage the work schedules and assignments of the clinical research staff.
•Track and report on the completion of research milestones and metrics.
•Assist the purchase, import, management of study materials and equipment.
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