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Administracja biurowa » Pracownik biurowy

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Opis:

Senior CRA oncology- global pharma company Nr ref.: /JOBS.pl A prestigious global pharma company, with a solid record of growth and strong pipeline of projects is seeking an experienced Senior Clinical Research Associate to join their organisation in Poland on a permanent basis. The position can be home based anywhere in Hungary or office based in Budapest.Responsibilities:Working fully outsourced to and based at the offices of our global pharmaceutical client, the Clinical Research Associate is ultimately responsible for the successful management of investigator sites throughout the site lifecycle, whilst working in accordance with ICH-GCP guidelines, the study protocol, applicable local and international regulatory requirements and internal Standard Operating Procedures.With full ownership of investigator sites for your assigned studies, your involvement begins at site feasibility stage, with responsibility for the successful management of the site right through to close-out. In addition to planning and conducting various site visits (feasibility, site selection, interim and close-out) in accordance with the clinical monitoring plan, you will foster effective relationships with investigator site staff to ensure that key clinical metrics are met. This will involve establishing innovative ways of increasing site and patient recruitment. When issues do occur, the Clinical Research Associate proactively and promptly implements corrective action plans, and, when applicable, escalates issues to more senior members of the study team. You may also design and deliver training to site staff, when appropriate.Typical duties will likely include preparing for and attending investigator meetings, coordinating the timely shipment and the subsequent proper storage and accountability of clinical supplies and following-up of drug safety issues that have occurred at your site. You will ensure the integrity of clinical data through your ability to sufficiently maintain site tracking records and work diligently to relevant guidelines.Through your ability to operate as a key part of a global study team, you will play a fundamental role in our client's drug development process.Qualifications:The successful candidate for this role will be able to demonstrate prior experience of working in investigator site management, including conducting monitoring visits, from either a pharmaceutical company or a CRO environment. It is essential that you have prior working knowledge of ICH-GCP guidelines and local and international regulatory requirements. Fluency in English is an absolute requirement, as well as an ability to communicate effectively with others and manage your time effectively.In return my client can offer a competitive salary and remuneration package, excellent career progression opportunities due to the unprecedented growth the company is currently experiencing and flexible working conditions.You can apply for this role by e-mailing your CV to Agata Wasko at or telephoning (0) Kontakt: Aplikuj teraz Ogłoszenie pochodzi z serwisu Jobs.pl .

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