Safety Issues Jobs in Bucharest

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 Physician More...

Triages incoming SAE information in order to fulfill timely reporting according to the authority/regulatory requirements.Participate in safety surveillance activities for assigned products; and also in area projects/goals. Identify and escalate problems to manager.Collecting analyzing More...

For our clientsTo 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 causal More...

Triages incoming SAE information in order to fulfill timely reporting according to the authority/regulatory requirements.Participate in safety surveillance activities for assigned products; and also in area projects/goals. Identify and escalate problems to manager.Collecting analyzing More...

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

Triages incoming SAE information in order to fulfill timely reporting according to the authority/regulatory requirements.Participate in safety surveillance activities for assigned products; and also in area projects/goals. Identify and escalate problems to manager.Collecting analyzing More...

Triages incoming SAE information in order to fulfill timely reporting according to the authority/regulatory requirements.Participate in safety surveillance activities for assigned products; and also in area projects/goals. Identify and escalate problems to manager.Collecting analyzing 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...

Req ID:492704At Alstom we understand transport networks and what moves people. From high-speed trains metros monorails and trams to turnkey systems services infrastructure signalling and digital mobility we offer our diverse customers the broadest portfolio in the industry. Every day More...

Req ID:491766At Alstom we understand transport networks and what moves people. From high-speed trains metros monorails and trams to turnkey systems services infrastructure signalling and digital mobility we offer our diverse customers the broadest portfolio in the industry. Every day More...

Req ID:491358At Alstom we understand transport networks and what moves people. From high-speed trains metros monorails and trams to turnkey systems services infrastructure signalling and digital mobility we offer our diverse customers the broadest portfolio in the industry. Every day More...

Req ID:490330At Alstom we understand transport networks and what moves people. From high-speed trains metros monorails and trams to turnkey systems services infrastructure signalling and digital mobility we offer our diverse customers the broadest portfolio in the industry. Every day More...

DescriptionPush boundaries. Explore ideas. Reshape tomorrow. Join Garrett and grow your career while helping top vehicle brands accelerate towards a cleaner safer and smarter future.Garrett is a cutting -edge technology leader delivering differentiated solutions for emission reduction More...

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/ 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...

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...

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...