Clinical Trials Jobs in Bosnia and Herzegovina

This is a great entry-point for detail-oriented professionals looking to launch a career in clinical research. As a TMF Assistant you will become the guardian of study integrity mastering the gold standard of clinical documentation.About the Role:Launch Your Career: Perfect for new starters to learn...

For the Client:To review and approve post-marketing Individual Case Safety Reports (ICSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment. The review includes coding seriousness assessment Company causality and comment listedness/expectedness an...

For the Client:To review and approve post-marketing Individual Case Safety Reports (ICSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment. The review includes coding seriousness assessment Company causality and comment listedness/expectedness an...

Job OverviewPerform daily administrative activities in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams to ensure a complete and accurate Trial Master File delivery.Essential Functions Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU) tea...

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and well-being.Responsibilities:Serve as medical point of contact for internal project team study sites and study sponsor for medical matters rela...

We are looking for a pharmacovigilance medical writer to join our team. The  Medical Writer will be responsible for medical writing including:PSURs/PBRERsPADERsACOsDSURsRMPsQC and review of all written output from the operations team as requiredSupporting the project managers to determine scheduling...