Clinical Research Associate

Strategically expanding European fast growing pharmaceutical clinical research organization is looking to expand their team.
This is a brand new opportunity for somebody, who wants to grow in career and join European leader who really looks after its employees.

Responsibilities:
­ Conducting Site initiation and Monitoring
­ Training of investigators/site staff during Site Initiation visits
­ Conducting Monitoring Visits in accordance with applicable SOPs/SSPs
­ Maintaining all files and documentation pertaining to studies
­ Motivating and support investigators/sites to achieve recruitment targets
­ Completing accurate study status reports
­ Ensuring study drug accountability verification in accordance with applicable SOPs/SSPs
­ Communicating study issues with directors/managers of Argint and Clients of Argint
­ Processing case report forms to quality standards
­ Coordinating the archiving of study files
­ Maintaining confidentiality of the clinical trials
­ Co-operating with QA/regulatory personnel during audits and inspections
­ Regulatory submissions to Competent Authorities
­ Submissions to Ethics Committees
­ Translation, verification and back translation of study documents

If you meet requirements stated above, please send us your CV in English language