Summary
M42 describes Danat Al Emarat as a specialist women’s and children’s hospital in Abu Dhabi. The Research Coordinator manages clinical studies and trials, supporting investigators and coordinating participant visits, consent, study documentation, and research data. The role also involves GCP and ethics compliance, participant safety reporting, audits, progress tracking, and sharing research findings. A bachelor’s degree in a healthcare-related field is required.
The posting
As published on m42.ae. Pulled from the employer's site and shown as they wrote it.
Overview
M42 delivers comprehensive healthcare services across the full continuum of care; from primary care to advanced specialty treatments. Leveraging cutting-edge health technologies and precision medicine, we ensure the highest standards of effectiveness, efficiency, and patient-centered outcomes. With a global presence spanning more than 480 facilities in 27 countries and a dedicated workforce of over 20,000 professionals, M42 is uniquely positioned to redefine the future of healthcare on a global scale.
Danat Al Emarat is a world-class specialty women’s and children’s hospital in the Emirate of Abu Dhabi. It offers advanced medical services across specialties including Neonatology, Pediatrics, Obstetrics & Gynecology, and Women’s Health. The hospital is one of the very few to encompass a dedicated Fetal Medicine Department along with a full-fledged Neonatal Intensive Care Unit (NICU) in the UAE. This has established Danat Al Emarat as a regional referral center for women with high-risk pregnancies, supported by its Level III NICU providing care for the most fragile newborns.
A Research Coordinator plays a key role in planning, coordinating, and managing research activities to ensure studies are conducted efficiently, ethically, and in compliance with regulatory requirements. In a healthcare or hospital setting, the Research Coordinator serves as the primary link between investigators, participants, clinical staff, and regulatory bodies, supporting the successful execution of research projects and clinical trials.
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.
- 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.
Bachelors Degree in any healthcare related field.