Clinical Research Associate

New position in Slovakia: CLINICAL RESEARCH ASSOCIATE (CRA)

Responsibilities
• Performing study feasibilities and Pre-Study visits in Slovakia and Czech Republic
• Cooperation with Regulatory Department with regards to regulatory submissions to Competent Authorities and Ethics Committees
• Assisting in the design of study documents including Master and Country-specific ICFs
• Translation, verification and back translation of study documents
• Training of investigators/site staff during Site Initiation visits
• Conducting Site initiation and Monitoring visits in Slovakia and Czech Republic
• 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

Qualification /Experience required
• minimum 2 years of experience in CRA position
• Medical/Science background and/or relevant experience
• Ability to review and evaluate clinical data
• Computer literacy
• Valid, clean driving licence
• Excellent communication skills
• Ability and willingness of traveling 50% of the working time

If you have excellent attention to detail, are organized and would enjoy being part of a friendly, professional and dynamic team, we'd love to hear from you.