Pain Management Jobs in Warsaw

The Pharmacovigilance (PV) Physician II is responsible for medical review of ICSRs and literature review writing signal detection reports supporting writing and or reviewing of aggregate reports (DSURS PSURS PBRERs PADERS). To review and approve post-marketing Individual Case Safety R More...

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 expectedness and Company causality as well as writing of More...

The Pharmacovigilance (PV) Physician II is responsible for medical review of ICSRs and literature review writing signal detection reports supporting writing and or reviewing of aggregate reports (DSURS PSURS PBRERs PADERS). To review and approve post-marketing Individual Case Safety R More...

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 expectedness and Company causality as well as writing of More...

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 expectedness and Company causality as well as writing of More...

Job OverviewLocation: home-based in Poland Senior Global Trial Managers (SGTMs) are an integral part of clinical trial delivery leading and working alongside clinical teams to improve patients lives by bringing new drugs to the market faster. The SGTM is a member of the core project t 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...

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...

IQVIA is searching for an experienced Clinical Product Specialist based in Poland on behalf of our client a growing medical devices company with a presence in over 90 countries. The company holds leading market positions in various categories including digestive health equipment and c More...