Senior Clinical Research Associate - FSP -

Covance is currently recruiting a Sr. CRA, ideally with expertise in Oncology (Phase I) and audits based at one of our clients' site in the region of Paris (91).  

This is the chance to join our CRO and a dynamic and supportive team! 

Responsibilites: 

• Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation
• Prepare accurate and timely trip reports
• Recruitment of potential investigators, preparation of EC submissions, notifications to regulatory authorities, translation of study-related documentation, organization of meetings and other tasks as instructed by supervisor
• Negotiate study budgets with potential investigators and assist the Covance legal department with statements of agreements as assigned
• Complete Serious Adverse Event (SAE) reporting, process production of reports, narratives and follow up of SAEs
• Audit follow-up 

What makes this job special? 

• Career progression will be exceptional because there are lots of studies coming through in 2019 across a variety of therapeutic areas You will be 100% client focused with a prestigious Pharmaceutical company Your Line Manager will be based in the Paris area too, there to support you where you need it

Other Information: This role is a full time & permanent position to be employed through Covance. For more information please contact Laetitia Chopin at laetitia.chopin@covance.com.