Clinical Research Associate

ARGINT INTERNATIONAL Clinical Research and Development Services Kft.

Place of work
Bratislava, Slovakia
Contract type

Information about the position

Job description, responsibilities and duties


• 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.

Salary information

2500-3500 EUR

Requirements for the employee

Candidates with education suit the position

University education (Bachelor's degree)
University education (Master's degree)
Postgraduate (Doctorate)

Educational Specialization


Language skills

English - Advanced (C1) and Slovak - Advanced (C1) and Czech - Advanced (C1)

Driving licence


Number of years of experience



Brief description of the company

◾Argint is a regional CRO providing clinical research services throughout Europe. We are focused on providing tailor made full-service solutions to small and medium sized biotech companies.
◾Argint was voted by members of the Pharma-IQ network as a ‘Top Ten’ CRO in 2016.
◾In September 2018, Argint joined Precision for Medicine, part of Precision Medicine Group.
◾Precision’s integrated set of capabilities across global clinical trial execution, sophisticated biomarker and specialty lab solutions will now be available to Argint’s clients to help address the many unique and complex challenges of bringing an innovative drug to market. In addition, by leveraging Precision’s extensive North American clinical trials footprint, Argint clients will now be able to conduct clinical trials in regions not previously available.
◾Together, Precision and Argint create a unique, fully-integrated solution to support the critical needs of emerging clients throughout Europe and North America in the rapidly-growing precision medicine space.

Number of employees

50-99 employees

Company address

Argint International s.r.o.
Galvaniho 7/D
82104 Bratislava


Contact person: Zsofia Mikola
E-mail: send CV
ID: 3700940   Datum zveřejnění: 23.6.2019   Základní složka mzdy (brutto) a další odměny:   2500-3500 EUR