Klinik Araştırma Saha Görevlisi

Atlas Cro Medikal Araş. ve Gel. Ltd. Şti

• Bachelors degree from universities Biology, Molecular Biology and Genetics, Nursing,Physics, Chemistry
• Good command of English both in writing and speaking
• Proficiency in MS Office (Word,Excel, Powerpoint)
• Analytical thinking, result and detail oriented
• Set, plan and accomplish goals under deadlines
• Mobile
• ICH-GCP domain preferable
• Knowledge about the clinical research
• At least 1 years experience in Site Coordinator

İŞ TANIMI

We are looking for Site Coordinator who are willing to make a career in clinical research sector. If you are interested in building your career in the clinical research please apply for this application.

• Support investigators in the protocol complience
• Support investigators in the informed consent process
• Support investigators actively in subject recruitment .(source data recording)
• Support investigators actively in the safety evaluation process
• Record subject data on CRFs if delegated by investigator
• Organise subject visit schedules according to the study protocol
• Filing all correspondences received from the sponsor and the ethics committee to the principal investigator's file
• Within the authorization of the coordinator physician, to help entering  data obtained from  volunteers completely and truly to printed or electronic case report forms (e-CRF) volunteer file and screening cards
• Sending blood samples drawn from volunteers to central or local laboratory as per the trial protocol, organization, tracking of courier procedures , monitoring laboratory reports, making the investigator  or physician or dentist examine reports, filing reports informing those concerned for taking immediate measure if there is a remarkable or labeled abnormal finding in the report.
• Taking necessary measures in order to ensure adequate amount of study materials,patient diaries , laboratory kits, patient identification cards and is available throughout the study.
• Relevant form for safety notifications which fulfill definition of serious adverse event reported by the volunteers is filled in by the investigator who is principal investigator or physician or dentist and it is immediately notified to the sponsor and monitoring such events.