Senior Clinical Research Associate

PSI CRO·Prague, Prague, Czechia

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About the role

Senior Clinical Research Associate responsible for onsite monitoring, study startup support, site communication and management, data review, quality control, regulatory support, and oversight of clinical research activities. The role requires independent monitoring experience in the Czech Republic, Phase II and/or III monitoring experience, fluency in Czech and English, a full clean driver’s license, and travel.

Key requirements

• BSc or MSc in Life Sciences (or similar), or an equivalent combination of education, training & experience
• Required skills: Independent on-site monitoring experience in the Czech Republic, Experience in all types of monitoring visits in Phase II and/or III, Strong written and verbal communication, Intermediate to Advanced knowledge of MS Office, Planning and multitasking, Communication, collaboration, and problem-solving, Ability to travel, Site communication and management, CRF review, Source document verification, Query resolution, Study startup support, Regulatory submission support
• Required languages: Czech, English
• Professional registration/licence (Czechia)

Opportunity details

• Workplace: On Site
• 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: Prague, Prague, Czechia

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.

Your responsibilities will include:

Conducting and reporting all types of onsite monitoring visits
Driving the study startup phase (if applicable)
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
Participating in feasibility research
Supporting the regulatory team in preparing documents for study submissions and regulatory approval

Qualifications

BSc or MSc in Life Sciences (or similar), or an equivalent combination of education, training & experience
Independent on-site monitoring experience in the Czech Republic, ideally on multiple projects at a time
Demonstrable experience in all types of monitoring visits in Phase II and/or III
Strong written and verbal communication skills
Fluency in Czech and English
Experience supporting Oncology studies is beneficial, but not essential
Intermediate to Advanced knowledge of MS Office
Ability to plan, multitask and work in a dynamic team environment
Communication, collaboration, and problem-solving skills are essential
As you will be monitoring multiple sites, you must have a full and clean driver's license, and the ability to travel.

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.