Contract Clinical Research Associate

PSI CRO·Vilnius, Vilnius County, Lithuania

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About the role

Contract Clinical Research Associate role based remotely in Lithuania, with onsite monitoring visits and travel required. Responsibilities include monitoring, CRF and source-document review, query resolution, site management, feasibility research, and regulatory submission support. Requires a Life Sciences college/university degree or equivalent education, training and experience, independent monitoring experience in Lithuania, English and Lithuanian proficiency, MS Office skills, and a valid driver’s license. Salary starts at €45 per hour.

Key requirements

• College/University degree in Life Sciences or an equivalent combination of education, training & experience
• Required skills: Independent monitoring experience in Lithuania, Conducting and reporting onsite monitoring visits, CRF review, Source document verification, Query resolution, Site communication and management, Vendor and in-house support coordination, Clinical study progress communication, Feasibility research, Regulatory document preparation, MS Office proficiency, Planning and multitasking, Communication, Collaboration, Problem-solving, Ability to travel, Valid driver's license
• Required languages: English, Lithuanian
• Professional registration/licence

Opportunity details

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

Full vacancy

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Employer’s role description

Job title: Contract Clinical Research Associate

Location: Vilnius, Vilnius County, Lithuania

Employment type: Full-time

Company Description

We are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global company founded in 1995, we bring together more than 3000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.

Job Description

As a Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry.

Remote opportunity in Lithuania

You will:

Conduct and report all types of onsite monitoring visits
Perform CRF review, source document verification and query resolution
Be responsible for site communication and management
Be a point of contact for in-house support services and vendors
Communicate with internal project teams regarding study progress
Participate in feasibility research
Support regulatory team in preparing documents for study submissions

Qualifications

College/University degree in Life Sciences or an equivalent combination of education, training & experience
Independent monitoring experience in Lithuania, preferably on contractor/freelance position
Full working proficiency in English and Lithuanian
Knowlegde of Latvian is a plus
Proficiency in MS Office applications
Ability to plan, multitask and work in a dynamic team environment
Communication, collaboration, and problem-solving skills
Ability to travel
Valid driver's license

Additional Information

We offer:

Flexible working conditions
Extensive training and friendly team
Opportunities for personal and professional growth
Competitive salary starting at 45 euro per hour. The precise salary depends on the specific qualifications and experience, and will be agreed upon on an individual basis.

If you feel it is time to make your skills and knowledge visible within a company with true focus on its people, then PSI CRO is the right choice for you.