Safety Program Jobs in Zagreb
Safety Program Jobs in Zagreb
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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...
Qualified Person Responsible For Pharmacovigilance Qppv In The Eu And Uk Homebased
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...
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 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...
Pharmacovigilance Physician Ii - Endocrincology Experience
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 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 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...
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...
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 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...
The European Institute of Policy Research and Human Rights is a prestigious institution that offers cuttingedge online programs designed to educate future leaders in policy research human rights and related disciplines. Our mission is to deliver worldclass skill enhancing programs to More...
Freelance Consultant 05 Fte Person Responsible For Local Literature Screening - Fluent In German
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 Senior Manager of Quality Management is responsible for leading one or more teams within Quality Management in line with global strategic objectives. The Senior Manager of Quality Management collaborates with global operational functions to ensure Pharmacovigilance and Medical Inf More...
Kao Prodajni savjetnik nauit e osnove voenja trgovine pridruiti se talentiranom timu novih prijatelja i to je najvanije nauiti kako da se nai kupci osjeaju dobrodolo sretno i nadahnuto dok u isto vrijeme ima priliku za izgradnju ivotne karijere.Kljune odgovornosti:Osigurava da su ku 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...
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