Clinical Research Coordinator
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 clinical research processes according to the research protocol;
- Identifying, pre-assessing, and enrolling study participants, and coordinating their participation in the study;
- Communicating with study participants, planning visits, and ensuring timely implementation of study procedures;
- Organizing the process of obtaining informed consent from study participants and producing relevant documentation;
- Ensuring compliance with the research protocol, ICH-GCP, local regulations, and SOPs defined within the study;
- Producing and managing study participants' medical and research documentation;
- Collecting, verifying, documenting, and timely entering study-related data into electronic/research systems (eCRF/EDC);
- Organizing study procedure results, laboratory and other test results, and ensuring relevant documentation;
- Ensuring confidentiality of study-related documents and protection of personal data;
- Timely identifying, documenting, and communicating possible protocol deviations to relevant individuals;
- Monitoring study timelines, participant visits, study procedures, and performance of relevant requirements;
- Preparing periodic reports and status reports related to study progress;
- Coordinating the management of necessary medications, biological samples, laboratory materials, and other resources within the study;
- Participating in the study completion/closure process and arranging relevant documentation;
Personal skills
- Ability to use time effectively;
- Teamwork skills;
Remuneration: (fixed) 1,275.00 GEL (accrued) + variable salary
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