Работа и карьера
Открыть поиск
Закрыть поиск
Clinical Research Coordinator (CRC)
24 Июнь 2025
Programmatic Positions
03 Апрель 2026
Regional Positions
03 Апрель 2026
Administrative Positions
03 Апрель 2026
Advance Team Support Positions
03 Апрель 2026
Ծրագրի Աշխատակից (Program Local Officer)
03 Апрель 2026
Ագրոնոմ
03 Апрель 2026
Loan Monitoring Senior Specialist
31 Март 2026
HR Assistant
31 Март 2026
SME Lending Senior Specialist
30 Март 2026
Driver
30 Март 2026
Տպագրիչ
28 Март 2026
Administrative Assistant
26 Март 2026
Call for Expression of Interest on Participatory Sense‑Making & Co‑Creation of Curricular Guidelines for Digital Literacy, Cybersecurity, AI Literacy and Soft Skills
26 Март 2026
Assistant Livelihood and Economic Inclusion Officer
26 Март 2026
Investigative Journalism Training Program on Combatting Corrosive Capital/Illicit Financial Flows/Strategic Corruption
25 Март 2026
Retail Products Development Specialist
24 Март 2026
Loan Officer
24 Март 2026
Վաճառողուհի
24 Март 2026
Հաշվապահ
24 Март 2026
Գնումների Մասնագետ
23 Март 2026
Ֆինանսիստ
23 Март 2026
Ֆինանսատնտեսական Բաժնի Պետ-Գլխավոր Հաշվապահ
23 Март 2026
Datacom Presales Specialist
23 Март 2026
Գործավար Սնանկության Գործերով Կառավարիչների Գրասենյակում
23 Март 2026
Տնօրենի Օգնական
19 Март 2026
Transport Operations Developer region Eurasia
19 Март 2026
Supply Chain Management Specialist
18 Март 2026
Medical Representative
19 Март 2026
Letter of Credit and Bank Guarantee Senior Specialist
17 Март 2026
Clinical Research Coordinator (CRC)
| Компания: | Representative Office of "KRKA, Pharmaceutical Factory, d.d., Novo Mesto" |
|---|---|
| Локация: | Yerevan, Армения |
| Крайний срок: | 24 July 2025 |
ОПИСАНИЕ ДОЛЖНОСТИ:
KRKA pharmaceutical factory is looking for an employee for the vacant position of Clinical Research Coordinator (CRC).The CRC will work with the authorized state body for IMPs approvals in Armenia, including the Ministry of Health, as well as doctors and lawyers, and will be responsible for the preparation of all documents necessary for the implementation of clinical trials (CT), obtaining the permission of CTs, and their implementation. for organization and monitoring.
The CRC must be able to propose, design, prepare, direct, coordinate, implement and monitor research-related activities and thus perform the work economically beneficial way and with optimum efficiency.
ОБЯЗАННОСТИ:
- Prepare clinical research documents with the head office of KRKA and submit them to the state authorized body for approval in order to obtain the certificates on time;- Organize, if necessary, tenders for contract research organizations or other companies involved in conducting clinical research (economically beneficial and with optimal efficiency);
- Ensure that clinical studies and related activities are performed in accordance with Good Clinical Practice, local laws and regulations, and corporate policies, procedures and Code;
- Prepare cost estimation for clinical study in a rational way and realization in an economical way and with optimal efficiency within the approved budget;
- Cooperate in the selection of proper investigator sites and investigators;
- Cooperate in organising investigator meetings;
- Ensure together with investigators the best recruitment practice for studies;
- Instruct research staff in scientific and procedural aspects of study management, including standards of care, informed consent procedures and documentation procedures (filling out/completing CRFs and other documentation);
- Collaborate in the management of day-to-day research-related activities, including problem-solving, protocol management, and communication with laboratories;
- Identify protocol violations, inform investigators of problems, or assist in problem resolution efforts such as protocol revisions;
- Be able to develop local Standard Operating Procedure (SOP) and be guided by it;
- Know the procedures for importing investigational pharmaceutical products (IMPs);
- Know the Armenian and European laws and guidelines regulating mining research;
- Create a clinical research budget and report regularly;
- Monitor clinical research and compile reports;
- Be able to perform multitasking within the set deadlines.
ТРЕБУЕМАЯ КВАЛИФИКАЦИЯ:
- Higher pharmaceutical or medical education;- Work experience in the field of clinical research will be an advantage;
- Excellent knowledge of Armenian, English and Russian languages;
- Ability to work effectively in a team;
- Excellent interpersonal, communication and networking skills;
- Computer skills (MS Word, MS Excel, MS Outlook and MS PowerPoint).
ПРОЦЕДУРА ПОДАЧИ ЗАЯВОК:
To apply, please send your CV to: ****.********@****.***Пожалуйста, четко укажите в своем заявлении, что вы узнали об этой возможности через Career Center, и укажите URL-адрес нашего веб-сайта - www.careercenter.am. Спасибо.
