Clinical Research Associate

PSI CRO · Belgrade, Serbia · posted Oct 2, 2026

Open to candidates in Bosnia and Herzegovina

Full-timejunior

You apply on the company's own site. We never charge to apply.

What this role actually asks for

Extracted by RemoteHunt

Must have

  • •College/University degree in Life Sciences
  • •At least 1 year of independent on-site monitoring experience
  • •Full working proficiency in English and Serbian
  • •Ability to travel across the region
  • •Valid driver’s license

Nice to have

  • •Experience in all types of monitoring visits
  • •Proficiency in MS Office applications

Tools and technologies

MS Office

Languages required

ensr

Worth checking before you apply

  • ⚠relocation required

The full posting

Company Description
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.

Job Description
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

Qualifications

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

Additional Information

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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