Senior Clinical Research Associate
Company: PSI CRO
Role summary
Senior Clinical Research Associate is a role at PSI CRO in Bratislava, Region of Bratislava, Slovakia (remote). Posted 2026-09-01. Experience level: 5-10.
- Job title
- Senior Clinical Research Associate
- Company
- PSI CRO
- Location
- Bratislava, Region of Bratislava, Slovakia
- Work arrangement
- remote
- Category
- Healthcare Support
- Experience level
- 5-10
- Date posted
- 2026-09-01
This is a fantastic opportunity for an experienced Clinical Research Associate to join a global company and make a real impact. You'll have the chance to work on exciting projects, collaborate with a supportive team, and grow your career in a dynamic environment. If you're looking for a role with great experience and a chance to advance, this could be the perfect fit.
Job description
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.