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Salary
≈ $26k – $65k per year (Estimated)
Location
Remote (Serbia)also open in Bosnia and Herzegovina
Seniority
Middle · 1+ year exp
Employment
Full-Time

Confirmed on the employer's own hiring board on Oct 14, 2026. First seen by Alion on Oct 2, 2026. PSI scores B on the Alion truth index.

Overview
Company
Impact
Profile match

PSI

PSI (PSI CRO AG) is a privately owned, global full-service contract research organization (CRO) headquartered in Zug, Switzerland, with significant operational hubs across North and South America, Europe, Asia-Pacific, and the Middle East. Founded in 1995, PSI specializes in providing clinical trial management, monitoring, regulatory affairs, biostatistics, data management, and medical writing services for global pharmaceutical, biotechnology, and medical device companies.

PSI is a leading Contract Research Organization with more than 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.

This position requires relocation to Trebinje area in Bosnia and Herzegovina.

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.

You will:

  • Conduct and report all types of onsite monitoring visits
  • Be involved in study startup
  • 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
  • Support and participate in audits and inspections
  • College/University degree in Life Sciences or an equivalent combination of education, training & experience
  • The candidate should meet the requirements for a CRA/monitoring position in Bosnia and Herzegovina
  • At least 1 year of independent on-site monitoring experience
  • Experience in all types of monitoring visits
  • Full working proficiency in English and Serbian
  • 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 across the region
  • Valid driver’s license

What We Offer:

  • Stability, long-term cooperation
  • Permanent contract, full-time job
  • Remote work setting
  • Car allowance, laptop and mobile phone
  • Career development
  • Unique combination of team collaboration and independent work
  • Friendly and supportive colleagues
  • Onboarding courses about clinical research industry
  • Mentoring and on-the job training
  • Comfortable office and team support in Banja Luka

This is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research.

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