Novella Clinical require an experienced CRA with a strong oncology/Medical Device background for a home based role in Belgium.
The CRA will work as part of an international clinical team which is led by the Clinical Trial Manager. The CRA is responsible for ensuring that, at the site level, the Clinical Monitoring Plan is implemented. The CRA will also ensure appropriate attention is provided to the sites in order to drive data quality so that the clinical study protocol requirements are fulfilled within the appropriate regulatory and ethical framework. Novella offers a dynamic and fast paced environment that allows you not only to utilise your current skill set and experience as well as to develop further.
Candidates must have the following skills and knowledge: Excellent knowledge of Good Clinical Practice (GCP) A good working knowledge of conducting clinical trials in general and specifically in oncology, ideally including haematological oncology (ie. Lymphomas, leukemias etc) Knowledge of local regulatory, ethics and institutional contract procedures and submissions Demonstrated experience of performing site start up procedures, routine monitoring and site closure Excellent interpersonal and organisational skills Ability to manage multiple priorities across various clinical trials Fluency in French or Dutch and English (spoken and written) is essential Valid drivers' licence and ability to travel throughout Belgium
Novella Clinical, a Quintiles company, is a full service, global CRO with European headquarters in Stevenage, UK. We are expanding our permanent work force in mainland Europe. This CRA role is permanent and full time.
To apply please send your English language CV in Word format to
Key words: CRA, SCRA, clinical research associate, senior clinical research associate, Sen CRA, Sen clinical research associate, France, French, oncology, haemato-oncology, haematological oncology, site manager.