Clinical Research Coordinator (Logistics)
Ogłoszenie mini
Gdańsk
Clinical Research Coordinator (Logistics)
Umowa o pracę
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Clinical Research Coordinator (Logistics)
Jestem
Firmą
Wymiar pracy
Pełny etat
Rodzaj umowy
Umowa o pracę
Branża / kategoria
Logistyka i planowanie
Poziom stanowiska
Specjalista
Requirements:
- Experience in logistics projects (planning, organization and control of logistics processes);
- English –intermediate (min. B2), other languages preferable;
- Polish (native);
- Knowledge of logistics processes, production planning and inventory management;
- Ability to identify dangerous goods as the first step to reduce the risk posed by the product with proper packaging, communication, handling and storage;
- Must possess excellent organizational skills and ability to work in a team;
- Resistance to stress and ability to work under time pressure;
- Ability to read and interpret documents, write routine reports and correspondence;
- Ability to calculate figures and amounts such as discounts, interest, commissions, proportions, percentages, circumference, and volume;
- Ability to apply concepts of basic algebra and geometry;
- Ability to apply common sense understanding to carry out instruction furnished in written, oral, or diagram form;
- Ability to deal with problems involving several concrete variables in standardized situations;
- Excellent analytical skills and good knowledge of MS Office (Word, Excel, and PowerPoint).
- Master of Science in Logistics and Supply Chain Management;
- Medical or clinical trials experience;
- IATA certification.
Summary of job: To provide logistical support for the project: checking, preparing shipments, monitoring shipments and resolving logistical problems. Responsible for working in accordance to actual regulatory guidelines and internal SOPs. Main tasks and responsibilities:
- Coordinating all logistic aspects of the projects;
- Preparing clinical studies logistic documentation;
- Reporting shipments delivery to the clients;
- Documenting all changes to the client in a timely manner (ex. NTFs for legal holidays, changes which occur during the clinical study, etc.);
- Archiving documents;
- Cooperating with clinical study investigators and project managers regarding logistic matters;
- Assisting the Analytical Project Manager in the coordination of supplies for each clinical study;
- Assessing Shipment/packages quality;
- Performing laboratory materials quality control prior shipment;
- Coordinating study samples logistic partially tested in other labs (affiliate, subcontracted, etc.);
- Completing all MICS forms related to logistic issues;
- Planning, conducting and documenting all study related logistics;
- Maintaining and developing clinical study related relationships with subcontracted labs and vendors
What we offer:
- Full-time job (Monday – Friday – 8h);
- Flexible working hours (you can start between 7:00 and 9:00);
- Contract of employment;
- Social benefits package (medical care, sports card subsidy, Benefit program);
- We will provide you with a comprehensive introductory training (min. 1 month), followed by the support of a mentor (Buddy).
Data dodania ogłoszenia: 10.06.2024
Aktualizacja: 29.06.2024
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Medicover Integrated Clinical Services
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Adres
Gdańsk
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