On behalf of a Contract Research Oganisation we are seeking a

Clinical Research Associate 

Responsibilities

• Independently performing all types of site monitoring and auditing duties according to ICH, GCP and SOPs (pre-study, initiation, interim and close-out).
• Providing training and/or guidance to site personnel.
• Reviewing the accuracy and completeness of regulatory documents at sites.
• Identifying and managing protocol deviations.
• Participating in the Serious Adverse Event (SAE) reconciliation process at sites.
• Distributing, filing and archiving clinical trial documents.

Requirements

• Medical doctor or pharmacist degree
• Min. 1 year experience as a Clinical Research Associate
• Fluency in Hungarian, and upper intermediate level of English knowledge
• Ability to work under limited supervision.
• Good problem solving skills.
• Willingness to travel.