Clinical Research Associate

Proclinical are currently recruiting for a Clinical Research Associate to be based in Zurich. The company is a multinational medical device manufacturer and are at the forefront of biomaterials, musculoskeletal, instruments and other orthopaedic technologies. The Clinical Research Associate will support on a temporary basis the Clinical Operations Department for clinical study planning, initiation, monitoring and management.

Job Responsibilities:

• Protocol development process + site selection process
• Contact selected sites and propose study participation, as needed
• Perform site selection visit according to standard internal procedures, as needed
• Drive and ensure timely completion of internal project and site approval process
• Drive contracting and payment processes during project duration
• Responsible to ensure timely initiation of the study and follow-up with site
• Support submission of protocols to ethics committees as needed
• Gather data and resolve data discrepancies as needed
• Perform statistics and write study report as needed

Skills and Requirements

• Previous experience in clinical study conduct activities is a must (1 year at least ideally)
• Strong knowledge of ISO, GCP, MedDev and MDR requirements related to Clinical Study preferred
• Fluent written and spoken German and English is a must

To Apply:

Please click on the Apply button. Please include a short note outlining why you are interested in the role and why you think you are suitable.
In case you have difficulty in applying or if you have any questions, please call Valaince Penteng on +44 203 8460 643 or upload your CV on our website - www.Proclinical.com.
A full job description is available on request.
Proclinical is a specialist employment agency and recruitment business, providing job opportunities within major pharmaceutical, biopharmaceutical, biotechnology and medical device companies.