Clinical Trials Jobs in Croatia

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...

The PV Associate should be a Life science / bio medical background graduate or have other healthcare related degree qualification (chemistry biology biotechnology veterinary science etc.) and be fluent in English and Slovenian. This is an opportunity for new graduates to start and develop their care...

Provide intelligence on requirements and contribute to the development of the strategy and set up activities including Regulatory Management Plan joint operating procedures POAs and core documents. Support identification of issues.Perform regular screening of regulatory legislative requirements upda...

Business Development Representative supports our Business Development team in building and expanding the network of clients.In this role you will Build and sustain long-lasting relationships with existing and potential clients (sponsors CROs medical institutions).Support Site Development Manager wit...

Assesses feasibility of research protocols based on knowledge and experience and in accordance with designated criteria to select the most suitable studies for the clinical site.  Supervises the conduct of clinical trials in accordance with ICH GCP applicable regulations procedures and protocols by...

Leads the team responsible for ICSR management for a selected project or group of projects as Team Leader Ensures adequate distribution of tasks for assigned projects and teams and oversees the workflow process Assures and exerts of activities leading to effective cooperation with clients in the are...

The PV Associate should be a Pharmacist. This is an opportunity for new graduates to start and develop their career within drug safety. The PV Associate will be working as part of a project team performing and supporting contracted pharmacovigilance activities on behalf of PrimeVigilance.  If you jo...

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...

Responsibilities include:To review and approve post-marketing Individual Case Safety Reports (lCSRs) and Serious Adverse Event (SAE) reports occurring in clinical trials for medical/causality assessment. Review includes coding assessment of seriousness listedness / expectedness and Company causality...