Safety Report Jobs in Zagreb

For the Client:To review and approve postmarketing 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/e More...

Job DescriptionThe Medical Reviewer II is responsible for medical review of lCSRs and literature review writing signal detection reports supporting writing and or reviewing of aggregate reports (DSURS PSURS/PBRERs/PADERS) as required by the Company or Client.For the Client:To review a More...

The Senior Pharmacovigilance (PV) Physician I is responsible for medical review of ICSRs writing and/or reviewing signal detection reports writing and or reviewing aggregate reports (DSURS PSURS PBRERs. PADERS) reviewing risk management reports (RMPs) and mentoring junior PV Phys More...

The Benefit/Risk Officer should be a Life science / bio medical background graduate preferably pharmacist with an experience in signal detection and use of signal management tools. The Benefit/Risk Officer will be working as part of a project team performing and supporting contracted More...

Qlik Sense Developer We are looking for a Qlik Sense Developer with 4 to 5 years of experience to join our team. The ideal candidate will be proficient in Qlik Sense both ClientManaged and SaaS versions as well as experienced with Nprinting. Strong English language skills are require More...

The EU QPPV is responsible for:The establishment and maintenance of a system which ensures that information about all suspected adverse reactions which are reported to the personnel of the Company and to medical representatives is collected and collated in order to be accessible at le More...

The Senior Pharmacovigilance (PV) Physician II is responsible for medical review of ICSRs writing and reviewing signal detection reports writing and/or reviewing aggregate reports (DSURS PSURS/PBRERs/PADERS ACOs responses to regulatory authority requests) writing and/or reviewing risk More...

The Medical Reviewer I is responsible for medical review of lCSRs and literature review writing of signal detection reports supporting writing and or reviewing of aggregate reports (DSURS PSURS/PBRERs/PADERS) as required by the Company or Client. Responsibilities include:To revie More...

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and wellbeing.Hybrid work in ZagrebResponsibilities:Medical point of contact for internal project team study sites and st More...

PSI Medical Monitors provide medical input to global clinical studies and advise the teams and business partners while always focusing on patients safety and wellbeing.Hybrid work in ZagrebResponsibilities:Medical point of contact for internal project team study sites and st More...

Gather and prepare data to support analytics from a variety of data sources including internal systems databases Excel spreadsheets and flat files as well as external sources if necessary  Create and maintain analyses reports and ad hoc report by using Power BI under Supervi More...

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.) This is an opportunity for new graduates to start and develop their career within drug safety. Th More...

The Senior PV Associate should be a Life science / bio medical background graduate or have other healthcare related degree qualification (chemistry biology biotechnology veterinary science etc.) This is an opportunity for new graduates to start and develop their career within drug saf More...

Assures and exerts activities leading to effective cooperation with clients in the area of literature monitoringContributes to achieving companys goals and objectivesEnsures that the Literature Screening responsibilities and activities are managed in a costefficient manner of the high More...

The PV Assistant will be working as part of a project team performing and supporting contracted pharmacovigilance activities on behalf of PrimeVigilance. Previous work experience in pharmacovigilance is not required as you will receive all necessary training from us. If you join More...

Assures and exerts activities leading to effective cooperation with clients in the area of literature monitoringContributes to achieving companys goals and objectivesEnsures that the Literature Screening responsibilities and activities are managed in a costefficient manner of the high More...

Location: Germany (Various Locations)We are seeking medical doctors specializing in internal medicine (m/f/d) with proficiency in German (at least B2/C1 level) to join leading German hospitals and occupational health centers. This opportunity is open to candidates within the EU and ou More...

The Senior PV Associate should be a Life science / bio medical background graduate or have other healthcare related degree qualification (chemistry biology biotechnology veterinary science etc.) This is an opportunity for new graduates to start and develop their career within drug saf More...

This is an exciting opportuniy for a freelancer / consultant to join our team as a Person Responsible for Local Literature Screening at 0.5 FTE.By working with us you will have the opportunity to work in an international team.Main responsibilitiesPerforming local scientific literature More...

The PV Assistant will be working as part of a project team performing and supporting contracted pharmacovigilance activities on behalf of PrimeVigilance. Previous work experience in pharmacovigilance is not required as you will receive all necessary training from us. If you join More...