法国关键人制药公司招聘肿瘤学临床研究博士后

2014年05月13日

来源：知识人网整理

摘要：

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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