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Z8RHSJM8 Posted 7 Oct Views: 37

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₾1275 / month Apply by 5 Nov

Translated automatically from the original posting. Read the original in Georgian →

"Caucasus Medicine Center" is a JCI-accredited, multi-profile, leading referral hospital in the region. It is staffed with the country's leading professionals and provides high-standard, high-tech medical services. The hospital's mission is to improve the quality of life of employees, patients, and the community, and to create the best medical experience.

At "Caucasus Medicine Center", we are looking for a new team member: a Clinical Research Coordinator.

Workplace: Tbilisi, Petre Kavtaradze #23 Schedule: 8 hours, 5 working days a week.

Requirements: - At least 1 year of experience in the field of clinical research is desirable; - Higher education in medicine, pharmacy, nursing, public health, biology, or a related field is desirable;

Main duties and responsibilities: - Planning, organizing, and coordinating daily processes of clinical research in accordance with the research protocol; - Identification, pre-assessment (screening), involvement, and coordination of the process of participants' involvement in the study; - Communication with study participants, planning visits, and ensuring timely implementation of research procedures; - Organization of the process of obtaining informed consent from study participants and production of relevant documentation; - Compliance with the requirements of the research protocol, ICH-GCP, local regulations, and SOPs defined within the study; - Production and management of medical and research documentation of study participants; - Collection, verification, documentation, and timely input of research-related data into relevant electronic/research systems (eCRF/EDC); - Organization of results of procedures conducted within the study, laboratory and other tests, and provision of relevant documentation; - Ensuring confidentiality of research-related documents and protection of personal data; - Timely identification, documentation, and communication with relevant persons regarding possible protocol deviations; - Monitoring study deadlines, participant visits, research procedures, and fulfillment of relevant requirements; - Preparation of periodic reports and status reports related to the progress of the study; - Coordination of the process of managing necessary medications, biological samples, laboratory materials, and other resources within the study; - Participation in the process of study completion/closure and arrangement of relevant documentation;

Personal skills: - Ability to use time effectively; - Teamwork skills;

Remuneration: (fixed) 1,275.00 GEL (accrued) + variable salary

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