Research Coordinator

About the role

The Research Coordinator will support the planning, execution, and management of clinical research studies at Danat Al Emarat, a leading women’s and children’s hospital in Abu Dhabi. This position acts as the primary liaison between investigators, participants, clinical staff, and regulatory bodies to ensure studies are conducted efficiently and ethically.

Key responsibilities

• Coordinate and manage clinical research studies and trials in line with approved protocols, including scheduling participant visits and collecting data.
• Obtain and document informed consent, maintain regulatory binders, and submit required documentation to IRBs/Ethics Committees.
• Monitor participant safety, report adverse events, and ensure compliance with Good Clinical Practice (GCP) and hospital policies.
• Facilitate site visits, audits, and inspections by sponsors or regulatory authorities, and prepare progress reports for investigators and sponsors.

Required profile

• Bachelor's degree in a healthcare‑related field.
• Experience supporting investigators and research teams in a hospital or clinical setting is preferred.