Research Coordinator

Responsibilities

• Coordinate and manage clinical research studies and trials in accordance with approved protocols.
• Assist Principal Investigators (PIs) and research teams with study planning, implementation, and completion.
• Obtain and document informed consent from study participants.
• Schedule participant visits, follow-ups, assessments, and research-related procedures.
• Collect, verify, maintain, and manage research data accurately and confidentially.
• Ensure compliance with hospital policies, ethical standards, Good Clinical Practice (GCP), and regulatory requirements.
• Prepare and submit research documentation to Institutional Review Boards (IRBs)/Ethics Committees.
• Maintain study files, regulatory binders, and essential research documents.
• Monitor participant safety and report adverse events or protocol deviations as required.
• Coordinate with physicians, nurses, laboratory personnel, pharmacists, and other departments involved in research activities.
• Manage study budgets, supplies, equipment, and research-related resources when applicable.
• Facilitate site visits, audits, monitoring visits, and inspections by sponsors or regulatory authorities.
• Track study progress, participant enrollment, and data quality to ensure study milestones are achieved.
• Prepare reports, study updates, and research summaries for investigators, sponsors, and hospital leadership.
• Provide education and guidance to research staff regarding study procedures and protocol requirements.
• Ensure confidentiality and secure handling of patient and research information.
• Support publication activities, presentations, and dissemination of research findings.
• Contribute to the development of evidence-based practices and continuous improvement in patient care through research initiatives.
  

Qualifications

• Bachelors Degree in any healthcare related field.