Key People have an exciting opportunity for an office based Clinical Research Associate focusing on Oncology studies to work for our biotech client based in Paris. 

Responsibilities: 

*Implement, follow and monitor the clinical trials in France 

*Participate to investigational site selection and site contract negotiation 

*Support the Clinical Project Manager in international coordination of clinical trials and IRB submissions 

*Participate to the writing and preparation of the essential document templates 

*Ensure that study documentation is completed and properly maintained in accordance with all applicable regulations 

*Monitor Investigational Medicinal Products (shipment, accountability, return and documentation) 

*Prepare and submit appropriate site visit reports within timelines 

*Provide regular study updates to company management and update tracking tools 

Requirements: 

*BS, BSN or RN 

*Qualified CRA with 2 to 5 years of field monitoring experience in phase 2 and 3 studies

*Oncology monitoring experience is a plus 

*Strong knowledge of regulatory environment 

*Computer proficient with the Microsoft Office suite of tools 

*Fluent in English 

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