Clinical Development Jobs in Wrocław

The Medical Director will lead educate mentor and develop the team of PV physicians to ensure their competence and confidence in developing their skills to become subject matter experts in pharmacovigilance. The role requires active monitoring of costs and project deliverables and int More...

Cloud Senior ManagerLocation: Wrocław / Katowice - 2 days office/3 days remoteLet us introduce you the job offer by EY GDS Poland a member of the global integrated service delivery center network by EY.The opportunityWere looking for a Head of Cloud Department with expertise in Techn More...

The Medical Director will lead educate mentor and develop the team of PV physicians to ensure their competence and confidence in developing their skills to become subject matter experts in pharmacovigilance. The role requires active monitoring of costs and project deliverables and int More...

The Executive VP Pharmacovigilance (PV) Operations is responsible for leading and overseeing all operational aspects of global pharmacovigilance activities ensuring compliance with regulatory requirements company SOPs and industry standards. This role will manage PV teams optimize ope More...

Main Purpose of RoleTo centrally manage a Lean and compliant Quality Management system for medical devices schemes (Medical includes Notified Body NB1639 UKCA ISO 13485 MDSAP and all other Medical Schemes at SGS)Management of external audits and communication with competent authorityM More...

 We are seeking a highly skilled Regulatory Manager to oversee the clinical and performance evaluation components of our medical device conformity assessment process within Notified Body 1639. This role is vital to ensuring regulatory excellence clinical integrity and t 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...

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...

The Medical Director will lead educate mentor and develop the team of PV physicians to ensure their competence and confidence in developing their skills to become subject matter experts in pharmacovigilance. The role requires active monitoring of costs and project deliverables and int More...