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- Senior Pharmacovigilance Specialist role focused on managing safety submissions, regulatory intelligence, and pharmacovigilance systems. The position involves overseeing ICSR submissions, periodic safety reporting, regulatory compliance activities, and system testing across...PredloženoRad u kancelariji
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- ...Alimentiv seeks a Senior Clinical Research Associate for its Belgrade office to independently manage clinical trial monitoring and site oversight across Serbia and Croatia. This individual contributor role involves site qualification, protocol compliance, data integrity oversight...PredloženoRad na daljinuRad u kancelariji
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- ...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...PredloženoPuno radno vremeStalno zaposlenjeRelokacijaRad na daljinuRad u kancelariji
- The FTE Medical Writer will serve as an integrated member of the team, delivering medical writing services for the development of clinical documents, including Clinical Trial Reports (CTRs), Trial Design Outlines/Clinical Trial Protocols (TDOs/CTPs) and CTP amendments, Briefing...PredloženoHitan početakPuno radno vreme
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