SMO UCT – Unit of Clinical Trials – is a dynamically developing company, which exercises control over the conduct of clinical trials of pharmaceutical products throughout the territory of Ukraine and abroad. One of the main tasks of the SMO UCT is to attract and develop highly qualified team of employees, who will be able to achieve professional success together. Therefore, if you are young, active and feel that you meet our requirements, if you want to work and earn money, send us your CV:
| Vacancy | Study site coordinator | |
| Region | Kremenchug | |
| Requirements | - Facilitate (conduct) trials according to GCP, regulatory requirements and local legislation, as well as the relevant standard operating procedures (SOPs); - Monitor the performance of research protocol procedures; - Be responsible for the the clinical trial quality; - Assist planning of audits in clinical trials; - Promptly send documents on the study of contact research organization (via email, fax or courier); - Maintain file of the clinical trial project and the file of center for clinical (CCS). - Hold responsibility for the preparation of documents by researchers submitting for the study submitting to the Department of Regulatory Affairs and CROs logistics; - Keep drug and other study materials accountability; - Сosts сontrol (remainder) of material assets received or acquired for clinical trials; Control the expenditure (balance) of received or acquired material assets for clinical trials conducting; | |
| Responsibilities | - Facilitate (conduct) trials according to GCP, regulatory requirements and local legislation, as well as the relevant standard operating procedures (SOPs); - Monitor the performance of research protocol procedures; - Be responsible for the the clinical trial quality; - Assist planning of audits in clinical trials; - Promptly send documents on the study of contact research organization (via email, fax or courier); - Maintain file of the clinical trial project and the file of center for clinical studies (CCS). - Hold responsibility for the preparation of documents by researchers submitting for the study submitting to the Department of Regulatory Affairs and CROs logistics; - Keep drug and other study materials accountability; - Сosts сontrol (remainder) of material assets received or acquired for clinical trials; Control the expenditure (balance) of received or acquired material assets for clinical trials conducting; | |
| Working Conditions | • Competitive and timely wages; • convenient work schedule; • formal employment; • corporate training/ seminars; • Opportunity for professional growth and career development; • young and friendly staff. | |
