Clinical Research Associate
Posted 23 days agoConfirmed open 32 min ago
Who can apply
Serbia only
Salary
Not disclosed
Level
Entry level
Full-time
Timezone
Not stated
About the role
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.
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.
Skills mentioned
Interested in this role?
You apply directly with PSI CRO. Remotavia never charges candidates.
Check your resume
See which keywords from this job your resume is missing.
Track this application
Add it to your board and get a follow-up reminder.
Draft a cover letter
An honest first draft from your resume and this job.
Prepare for interviews
Likely questions based on this job description.
About PSI CRO
Listing details & historyShowHide
- Employer posted
- 2 Oct 2026
- Last confirmed open
- 32 min ago
- Source
- Employer careers site
- Degree
- Degree required
- “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 Pa”
- Visa
- Not stated
- Timezone
- Not stated
- Languages
- English
- Location evidence
- “Remote (Belgrade, Serbia)”
Details are read from the listing text. They are not a guarantee of work authorization; confirm with the employer.