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- Clinical Regulatory Affairs Associate
HAYS Poland Sp. z o.o.
Clinical Regulatory Affairs Associate
- Data publikacji:
- 12.3.2010
- Miejsce pracy:
- cała Polska
Od kandydatów oczekujemy:
- Main Responsibilities:
- EC submissions ( Preparing and completing EC application forms, SIS/IC, Study synopsis and other required documents according to the EC specific requirements and company SOP in collaboration with the project team)
- Participate in Kick-off Meetings
- Undertake other reasonably related duties as may be assigned from time to time.
Oferujemy:
- Essential requirements:
- Minimum 1 year of relevant experience in clinical research
- Medical/science background and/or relevant experience
- Ability to liaise with other departments and Project Teams across European offices
- Be able to demonstrate an understanding of regionally specific legislation surrounding ethics committees and submissions procedures and practices
- Excellent interpersonal and presentation skills and the ability to interact at all levels
- Be able to demonstrate a thorough understanding of ICH as well as having both pre-clinical and clinical knowledge
- Fluent English
- Do not hesitate to email your CV to agnieszka.pastula@hayspharma.com
Prosimy o dopisanie w CV następującej klauzuli "Wyrażam zgodę na przetwarzanie moich danych osobowych zawartych w mojej ofercie pracy dla potrzeb niezbędnych do realizacji procesu rekrutacji (zgodnie z ustawą z dn. 29.08.97 roku o Ochronie Danych Osobowych Dz. Ust Nr poz. 883)".