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JOB DETAILS

Senior Clinical Research Associate

CompanyPSI CRO
LocationBratislava
Work ModeRemote
PostedSeptember 1, 2026
About The Company
PSI is a leading full-service global Contract Research Organization whose key strength is predictable patient enrollment across multiple therapeutic areas. PSI is known in the industry as a CRO focused on ‘on-time project delivery’. This is achieved through investing substantial effort and MD resources into performing quality feasibility assessments that provide an accurate predictor of study timelines. PSI’s global reach allows us to run clinical trials across multiple continents, in 50+ countries around the world. PSI’s reputation is that of a 'no-nonsense'​ CRO focused on timely patient enrollment and project delivery. An exceptionally high repeat and referral business rates alongside low staff turnover are indicative of our commitment to be the best CRO in the world as measured by our clients and our employees. http://www.psi-cro.com
About the Role

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.

Key Skills
Clinical researchOn-site monitoringCRF reviewSource document verificationQuery resolutionSite managementOncologyGastroenterologyClinical trial complianceCommunicationProblem-solvingMS Office
Categories
HealthcareScience & Research
Benefits
Professional developmentCareer growth opportunities
Job Information
📋Core Responsibilities
The Senior CRA is responsible for conducting onsite monitoring visits, performing source document verification, and ensuring data quality and compliance. They also manage site communications, oversee study timelines, and act as a primary point of contact for project stakeholders.
📋Job Type
full time
📊Experience Level
5-10
💼Company Size
2956
📊Visa Sponsorship
No
💼Language
English
🏢Working Hours
40 hours
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