Experienced CRA – Clinical Research Associate ()
Beschrijving:
- You are responsible for the management and monitoring of different phases, especially phase IV trials.
- You act as the main line of communication between the sponsor and the investigator
- You ensure delivery of high quality, clean CRFs by adherence to Good Clinical Practices and ensuring investigator compliance with protocol and study procedures
- You ensure adequacy of clinical research staff/facilities in accordance with defined general (GCP/ Sops) and protocol-specific requirements
- You ensure timely submission, initiation, monitoring and close-out
- You ensures investigator completion and compilation of all necessary pre-trial documentation from the investigator site (e.g. signed protocol, Cvs, patient information and consent forms, ethics committee approval documents etc.)
- You may Negotiate investigator grants within a protocol specific budget suggested by Clinical Operation Management
- You perform and coordinate trial specific training for investigational site staff
- Scientific Degree or experience in the conduct of clinical trials
- A good knowledge of English, Dutch and French is an absolute requirement
- Experience in a similar position is an absolute requirement
- Experience with Microsoft based applications and general knowledge of PC functions
- A contract of indefinite duration
- The opportunity to develop your competences and grow your career within a dynamic and challenging leading company
- You will receive an attractive salary with other advantages as e.g. group insurance, hospitalization insurance, meal vouchers, Company Car, …
- You will have the ability to work partially home based
Categorie:
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