Clinical Research Associate

I have a fantastic opportunity for a Clinical Research Associate (CRA) with my client in Zurich, Switzerland.

CRA Responsibilities:
*Study Feasibility
*Study set-up
*Document Management
*Study site staff
*Monitoring

CRA Requirements:
*Monitoring Phase II and Phase III trials
*Establish and maintain relationships with internal/external contacts
*Prepare high quality documents for submission to Ethics Committees and Regulatory Authorities
*Track and plan regulatory activities to meet agreed timelines
*Maintain a current awareness of ethical and regulatory requirements
*Report writing skills
*Effective verbal and written communication in individual and group settings
*Ability to create and maintain relationships with internal/external contacts
*Deliver high quality customer services to internal/external customers
*Ability to source information, research skills
*Ability to analyse and interpret data
*Problem solving skills
*Excellent attention to detail
*Ability to work in a team environment
*Ability to plan, organise and follow up
*Effective time management of multiple tasks
*Negotiation skills
*Presentation skills
*Computer literacy

If this permanent position is of interest to you please send your CV through ASAP.

Abraxas plc is a leading specialist recruitment agency for the IT industry. Abraxas is also one of the founding members of The Association of Professional Staffing Companies (APSCo). Due to the high level of applications we receive, please be aware that you may not hear from us immediately, as we can only respond to those applicants whose skills and qualifications are suitable for this position. If you would like Abraxas to help you find a similar position, or for a complete listing of all our current vacancies, please visit our website at www.abraxas.com and register your details. Please note that no terminology in this advert is intended to discriminate on the grounds of age, and we confirm that we will gladly accept applications from persons of any age for this role.