Senior Clinical Research Associate

PSI CRO·Bratislava, Bratislava Region, Slovakia

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About the role

PSI seeks a freelance, contractor Senior Clinical Research Associate working home-based from within Slovakia. The role involves onsite monitoring visits, CRF and source document review, query resolution, site management, study timeline oversight, vendor coordination and quality control. A life sciences degree or equivalent experience, independent monitoring experience in Slovakia, Phase II/III monitoring experience, Slovak and English fluency, a valid driver’s license and travel ability are required.

Key requirements

• BSc or MSc in Life Sciences (or similar), or an equivalent combination of education, training & experience
• Required skills: Independent on-site monitoring in Slovakia, All types of monitoring visits in Phase II and III, Clinical site communication and management, CRF review, Source document verification, Query resolution, Study activity, timeline and schedule supervision, Vendor and in-house support coordination, Quality control and compliance monitoring, MS Office at intermediate to advanced level, Communication, Collaboration, Problem-solving, Ability to travel
• Required languages: Slovak, English
• Professional registration/licence (Slovakia)

Opportunity details

• Workplace: Hybrid
• Employment: Contract
• Posted: Sep 15, 2026
• Original advert language: English

Full vacancy

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Employer’s role description

Job title: Senior Clinical Research Associate

Location: Bratislava, Bratislava Region, Slovakia

Employment type: Full-time

Company Description

PSI is a leading Contract Research Organisation with 30 years in the industry, offering a perfect balance between stability and innovation to both clients and employees. We focus on delivering quality and on-time services across a variety of therapeutic indications.

Job Description

As a Senior CRA, you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications. You will build and maintain relationships with clinical sites and investigators. Your focus will be on subjects’ rights, safety and well-being and quality of data compliance.

This is a freelance (contractor) home-based position from within Slovakia.

Your responsibilities will include:

Conducting and reporting all types of onsite monitoring visits
Performing CRF reviews, source document verification and query resolution
Be responsible for site communication and management
Supervising study activities, timelines, and schedules for each site
Acting as a point of contact for in-house support services and vendors
Supporting quality control, such as compliance monitoring and reports review

Qualifications

BSc or MSc in Life Sciences (or similar), or an equivalent combination of education, training & experience
Independent on-site monitoring experience in Slovakia
Demonstrable experience in all types of monitoring visits in Phase II and III
Fluency in Slovak and English
Experience supporting Oncology and Gastroenterology studies is beneficial
Valid driver's license and the ability to travel
Intermediate to Advanced knowledge of MS Office
Communication, collaboration, and problem-solving skills are essential

Additional Information

Make the right call and take your career to a whole new level. Join the company that focuses on its people and invests in their professional development and success. Our recruitment process is easy and straightforward, and we’ll be there with you every step of the way. We will guide and support you with information, making your experience as smooth as possible.