Clinical Research Associate

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.