Job Title: Research Coordinator
Reports to: Research Manager
Location: Dubai
Job Summary:
GluCare Integrated Diabetes Center is looking for an organized and detail-oriented Research
Coordinator to manage and oversee the day-to-day activities of clinical research studies. The
Research Coordinator will ensure that studies are conducted in compliance with all relevant
protocols, regulations, and standards, while also supporting the clinical research team to achieve
the study’s objectives efficiently.
Key Responsibilities:
● Study Management: Coordinate and manage the operational aspects of clinical trials and
research studies, ensuring compliance with protocols.
● Patient Recruitment: Work closely with the clinical team to identify, recruit, and enroll
patients into research studies, ensuring informed consent is obtained.
● Data Collection: Supervise the collection, entry, and management of clinical data in accordance
with regulatory and institutional standards.
● Regulatory Compliance: Ensure all study activities comply with regulatory guidelines,
including ethical standards and clinical research policies.
● Documentation: Maintain accurate and up-to-date records, including participant files, study
documentation, and regulatory submissions.
● Monitor Study Progress: Track the progress of research studies, ensuring that milestones are
met on time and within budget.
● Communication: Liaise between study sponsors, researchers, and clinical teams to facilitate
communication and address any issues that arise.
● Training & Support: Train and support study staff in study procedures, including proper data
collection methods and compliance protocols.
● Quality Control: Ensure the quality and integrity of data by regularly reviewing study records
and conducting audits as required.
Qualifications:
● Bachelor’s degree in Life Sciences, Nursing, Public Health, or a related field (Master’s preferred).
● Previous experience as a Research Coordinator or in clinical research administration, ideally in a
healthcare setting.
● Familiarity with clinical research regulations and Good Clinical Practice (GCP) guidelines.
● Strong organizational and multitasking skills, with attention to detail.
● Excellent communication and interpersonal skills, with the ability to work with diverse teams.
● Proficiency in Microsoft Office and experience with clinical trial management systems (CTMS) or
electronic data capture (EDC) platforms is a plus.