 Најди Работа » Прегледај оглас
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Комак Медикал ДООЕЛ
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Регион:
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Скопски,
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Објавен од:
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Најди Работа,
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Објавувач:
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Комак Медикал ДООЕЛ
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Популарност на компанијата:
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Област:
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Медицина
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Работно Место:
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Координатор
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Број на работни места:
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1
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Тип на работно место (постојано времено):
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Времено
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Објавен на:
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17/11/2023
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Краен рок за пријавување:
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24/11/2023
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Оглас внесен на:
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16/11/2023
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Емаил:
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jobs@comac-medical.bg
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URL:
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https://comac-medical.com/
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Контакт телефон:
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Поштенски Фах:
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Адреса за апликација:
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jobs@comac-medical.bg
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Назнака (референца) на огласот:
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Site Coordinator
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Договор во месеци:
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6
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Почеток на работен однос:
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Плата:
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Должности:
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Нема информација,
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Потребни Квалификации:
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Graduate or postgraduate degree, preferably in the field of Biology, Pharmacy, Chemistry, Medicine, Dentistry or other relevant;
• One year of experience in the leading role in a clinical research filed;
• Very good knowledge of clinical research process;
• Sound knowledge of current ICH/GCP guidelines and country-specific regulations;
• Particularly good organizational and coordination skills;
• Excellent communication skills both written and spoken;
• Working knowledge of Word, Excel, and PowerPoint;
• Fluency in English language;
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Број на прегледи:
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568
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Целосен оглас:
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Great job opportunity for a SITE COORDINATOR for one of the most reputable, full-service providers of CRO and SMO
Established in 1997, with locations in Central & Eastern Europe and 290 full-time dedicated professionals, COMAC MEDICAL is a recognized leader in clinical research and provides innovative and non-conventional solutions of high quality for the pharmaceutical industry.
Currently, we are looking for a professional to coordinate clinical research studies activities, to streamline processes, administration and communication between teams involved in the study.
What is expected to be done?
• Support all types of feasibility inquiries at the respective site;
• Assist the site team with regards to subject pre-selection and recruitment;
• Help the site team in subjects’ visits planning and preparation;
• Organize various source of documentation;
• Complete Case Report Form and maintain Investigator Site File;
• Participate and coordinate any trainings and meetings (incl. Investigator Meetings) related to a specific study;
• Collaborate with the site team for any adverse events and safety information reporting and escalation;
• Organize and coordinate logistic of study medication, other study supplies and biological samples;
• Ensure timely site equipment maintenance and calibration;
• Handle subject expenses reimbursement;
• Support project team in the collection of site-specific documents;
• Support the site team in audit/inspection preparation, as needed
What is required for the role?
• Graduate or postgraduate degree, preferably in the field of Biology, Pharmacy, Chemistry, Medicine, Dentistry or other relevant;
• One year of experience in the leading role in a clinical research filed;
• Very good knowledge of clinical research process;
• Sound knowledge of current ICH/GCP guidelines and country-specific regulations;
• Particularly good organizational and coordination skills;
• Excellent communication skills both written and spoken;
• Working knowledge of Word, Excel, and PowerPoint;
• Fluency in English language;
Why join Comac Medical?
• Great team of knowledgeable, high-achieving and experienced professionals;
• International and diverse work atmosphere;
• Challenging projects in a different therapeutical area as well as in early phases;
• Opportunity to enrich professional skills and progress in career development;
• Competitive remuneration;
• Professional trainings;
Core strengths of Comac Medical
• Proven track record for quality and delivery;
• Established and trusted relationships with KOLs;
• Motivated, capable and dedicated team;
• Global full-service capabilities;
If you are interested, challenged, and convinced that the job opportunity is exactly for you, do not hesitate and send your detailed resume in English at jobs@comac-medical.bg
Only the shortlisted candidates will be contacted on time.
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